반응 #1497
ord-453ce30ee5274954b0f4cd3bf04e1207
반응 방정식
dimethylamino pyridine
ethyl acetate
5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-carboxylic acid
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
Compound E3
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
→
title compound
Benzyl-4-[[(5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-yl)carbonyl]oxy]-benzoate
반응물
dimethylamino pyridine
ethyl acetate
—
1-(3-dimethylaminopropyl)-3-ethylcarboimide hydrochloride
5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-carboxylic acid
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
Compound E3
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
—
benzyl 4-hydroxy benzoate
시약
없음
반응 조건
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.STIRRINGstirred at ambient temperature for 16 hours
- 2세척washed with water (10 mL), brine (10 mL)
- 3기타dried
- 4workup.DISTILLATIONsolvent distilled off
실험 절차
To a solution of 5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-carboxylic acid (Compound E3, 386 mg, 1.77 mmol) in dimethylformamide (4 mL) was added 1-(3-dimethylaminopropyl)-3-ethylcarboimide hydrochloride (440 mg, 2.3 mmol) followed by dimethylamino pyridine (DMAP) (280 mg, 2.3 mmol). The mixture was stirred for 10 minutes, and benzyl 4-hydroxy benzoate (426 mg, 1.9 mmol) was added and stirred at ambient temperature for 16 hours. The mixture was diluted with ethyl acetate (100 mL) and washed with water (10 mL), brine (10 mL), dried and solvent distilled off. The title compound was obtained as a pale yellow solid after chromatographic purification.