反応 #4160513
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-ee483b3361bf4aab813ec94ae2d4ab4f表示可能な構造データがありません
CC(C)(CO)C(C(=O)NC1CCCCC1)O製品情報
N-cyclohexyl-2,4-dihydroxy-3,3-dimethylbutanamide (CAS 16424-76-3) 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 289865
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
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ee483b3361bf4aab813ec94ae2d4ab4f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ee483b3361bf4aab813ec94ae2d4ab4f反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
ソース ID: ord-a2458d88773e4e84a76641c9464a3622反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
ソース ID: ord-a2458d88773e4e84a76641c9464a3622反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Place N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide (2.178 g, 9.51 mmol), triethylamine (2.7 ml, 19.31 mmol) and toluenesulfonyl chloride (3.70 g, 19.21 mmol) in CH2Cl2 (50 mL) at 0° C. Stir for 30 minutes at 0° C. Quench with hexane and warm to room temperature. Filter white precipitate. Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere. Add sodium hydride (3.4 g, 85 mmol) and stir at room temperature for 12 hours. Quench the reaction with methanol/water mixture. Extract with ethyl acetate. Wash the extract with brine and dry over magnesium sulfate. Purification by flash chromatography affords 1.25 g (36%) of the title compound: Mass spectrum (apci) m/z=366 (M+H). at 0° C Quench with hexane warm to room temperature Filter white precipitate Strip the solvent and dissolve the residue in 40 ml of dry THF under the nitrogen atmosphere Quench the reaction with methanol/water mixture Extract with ethyl acetate Wash the extract with brine dry over magnesium sulfate Purification by flash chromatography
ソース ID: ord-a2458d88773e4e84a76641c9464a3622反応条件: temp:150.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Place 2-hydroxy-3,3-dimethyl-cyclopentanone (1.044 g, 7.86 mmol), cyclohexylamine (1.91 ml, 16.51 mmol) and toluenesulfonic acid monohydrate (0.152 g, 0.1 mmol) in EtOH (4 mL) in a microwave reactor. Stir for 1 hour at 150° C. Quench with 1N HCl and extract with ethyl acetate. Wash the extract with NaHCO3, brine. Dry over magnesium sulfate, filter, and concentrate to afford N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide. Quench with 1N HCl extract with ethyl acetate Wash the extract with NaHCO3, brine Dry over magnesium sulfate filter concentrate
ソース ID: ord-97a5dda0d18c43b6a17d06eeefbf8222反応条件: temp:150.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Place 2-hydroxy-3,3-dimethyl-cyclopentanone (1.044 g, 7.86 mmol), cyclohexylamine (1.91 ml, 16.51 mmol) and toluenesulfonic acid monohydrate (0.152 g, 0.1 mmol) in EtOH (4 mL) in a microwave reactor. Stir for 1 hour at 150° C. Quench with 1N HCl and extract with ethyl acetate. Wash the extract with NaHCO3, brine. Dry over magnesium sulfate, filter, and concentrate to afford N-cyclohexyl-2,4-dihydroxy-3,3-dimethyl-butyramide. Quench with 1N HCl extract with ethyl acetate Wash the extract with NaHCO3, brine Dry over magnesium sulfate filter concentrate
ソース ID: ord-97a5dda0d18c43b6a17d06eeefbf8222PubChem References
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