反応 #4127811
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-78f098643ce64fbabbaaf9053f93d0e7表示可能な構造データがありません
COC(=O)CSCC#N製品情報
methyl 2-(cyanomethylsulfanyl)acetate (CAS 52069-53-1) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 2778540
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-78f098643ce64fbabbaaf9053f93d0e7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]-acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-52e98f09db22491e9c2b2841aada0cca反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]-acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-52e98f09db22491e9c2b2841aada0cca反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]-acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-52e98f09db22491e9c2b2841aada0cca反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-78f098643ce64fbabbaaf9053f93d0e7反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: - 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-d057f1c76ce24822956eec62a889d852反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]-acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-db02c3c015ab42b8a44766dc6c7607ff反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 G. (0.3 mol) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-1e9fa283e93c42a88feeabe0b435f3fe反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 31.8 g. (0.3 mol.) of thioacetic acid methyl ester are added to 150 ml. (0.3 mol.) of 2N sodium methylate solution. 22.6 g. (0.3 mol.) of chloroacetonitrile dissolved in 30 ml. of methanol are added dropwise while cooling and stirring. It is stirred overnight then refluxed for 30 minutes. The reaction mixture is cooled and the solvent is evaporated. 100 ml. of water are added to the residue and the aqueous solution is extracted twice with ether. The combined ether extracts are decolorized with activated carbon and dried with magnesium sulfate. The ether is distilled off and the residue is distilled under vacuum. 30.5 g. of 2-[(cyanomethyl)thio]-acetic acid methyl ester are obtained b.p.10mm 132°-134°. while cooling It is stirred overnight then refluxed for 30 minutes The reaction mixture is cooled the solvent is evaporated of water are added to the residue the aqueous solution is extracted twice with ether dried with magnesium sulfate The ether is distilled off the residue is distilled under vacuum
ソース ID: ord-52e98f09db22491e9c2b2841aada0ccaPubChem References
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