반응 #1497

ord-453ce30ee5274954b0f4cd3bf04e1207

반응 방정식

CN(C)c1ccccn1
dimethylamino pyridine
CCOC(C)=O
ethyl acetate
CC1(C)CCC(=O)c2cc(C(=O)O)ccc21
5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-carboxylic acid
CC1(C)CCC(=O)c2cc(C(=O)O)ccc21
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
CC1(C)CCC(=O)c2cc(C(=O)O)ccc21
Compound E3
CC1(C)CCC(=O)c2cc(C(=O)O)ccc21
5,5-Dimethyl-5,6-dihydro-naphthalen-8(7H)-one-2-carboxylic acid
CC1(C)CCC(=O)c2cc(C(=O)Oc3ccc(C(=O)OCc4ccccc4)cc3)ccc21
title compound
CC1(C)CCC(=O)c2cc(C(=O)Oc3ccc(C(=O)OCc4ccccc4)cc3)ccc21
Benzyl-4-[[(5,5-dimethyl-5,6,7,8-tetrahydro-8-oxo-naphthalen-2-yl)carbonyl]oxy]-benzoate

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirred at ambient temperature for 16 hours
  2. 2
    세척washed with water (10 mL), brine (10 mL)
  3. 3
    기타dried
  4. 4
    workup.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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723666uspto-grants-1998_03