反応 #4118643
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-f7c04016b5e0452388080ca7d82cfe26表示可能な構造データがありません
CCOC(=O)C(Cl)(Cl)Cl製品情報
ethyl 2,2,2-trichloroacetate (CAS 515-84-4) 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 10588
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f7c04016b5e0452388080ca7d82cfe26反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-71d708329f3446f59d5ae6e5af9cdbac反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5f282c9ef17241e19e49848e7bfe609a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 0.60 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 0.29 g of zinc dust and 10 ml of N,N-dimethylformamide was added ethyl trichloroacetate with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was poured into 10 ml of diluted hydrochloric acid and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over magnesium sulfate and then evaporated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.04 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3-chloro-3-ethoxycarbonyl-2-propenyloxy)butyloxy)benzene (yield, 5%), nD23.0 1.5348. After stirring at room temperature for 2 hours extracted twice with diethyl ether washed with water dried over magnesium sulfate evaporated to give a crude product
ソース ID: ord-5d15c627687f44229f5bee816b68686d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Ethanol is reacted with trichloroacetic anhydride to yield ethyltrichloroacetate.
ソース ID: ord-1d4b404771e248cdb8fa59d34b337750反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Ethanol is reacted with trichloroacetic anhydride to yield ethyltrichloroacetate.
ソース ID: ord-1d4b404771e248cdb8fa59d34b337750反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: In a 10 mL round-bottom flask, 1.88 g of diethyl ethylmalonate (10 mmol), 2.10 g of ethyl trichloroacetate (11 mmol), 158 mg of tetra-n-butylammonium fluoride trihydrate (0.5 mmol), and 69 mg of potassium carbonate (0.5 mmol) were stirred at 24° C. for 5 h. After filtration, the solution was found to contain 1.56 g (70% yield) of diethyl α-chloro-α-ethylmalonate. After filtration
ソース ID: ord-bf9b038c957d4ccf9eda320c0a3fec1a反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 0.60 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 0.29 g of zinc dust and 10 ml of N,N-dimethylformamide was added ethyl trichloroacetate with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was poured into 10 ml of diluted hydrochloric acid and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over magnesium sulfate and then evaporated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.04 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3-chloro-3-ethoxycarbonyl-2-propenyloxy)butyloxy)benzene (yield, 5%), nD23.0 1.5348. After stirring at room temperature for 2 hours extracted twice with diethyl ether washed with water dried over magnesium sulfate evaporated to give a crude product
ソース ID: ord-5d15c627687f44229f5bee816b68686d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 0.60 g of 4-(2,6-dichloro-4-(3,3-dichloro-2-propenyloxy)phenoxy)butyloxyacetaldehyde, 0.29 g of zinc dust and 10 ml of N,N-dimethylformamide was added ethyl trichloroacetate with stirring at room temperature. After stirring at room temperature for 2 hours, the reaction mixture was poured into 10 ml of diluted hydrochloric acid and extracted twice with diethyl ether. The diethyl ether layers were combined, washed with water, dried over magnesium sulfate and then evaporated to give a crude product. The crude product was subjected to silica gel chromatography, which afforded 0.04 g of 3,5-dichloro-1-(3,3-dichloro-2-propenyloxy)-4-(4-(3-chloro-3-ethoxycarbonyl-2-propenyloxy)butyloxy)benzene (yield, 5%), nD23.0 1.5348. After stirring at room temperature for 2 hours extracted twice with diethyl ether washed with water dried over magnesium sulfate evaporated to give a crude product
ソース ID: ord-5d15c627687f44229f5bee816b68686d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Ethanol is reacted with trichloroacetic anhydride to yield ethyltrichloroacetate.
ソース ID: ord-1d4b404771e248cdb8fa59d34b337750反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f7c04016b5e0452388080ca7d82cfe26反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-71d708329f3446f59d5ae6e5af9cdbacPubChem References
化合物の公開データベース記録に掲載された情報源です。
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