تفاعل #1494
ord-bf2e44a5bdea4415bef84fd79bdef046
معادلة التفاعل
ethyl 2-bromoacetate
3,4-dihydro-4,4-dimethyl-7-bromo-naphthalen-1(2H)-one
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
Compound G
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
→
title compound
(±)Ethyl 2-(1-hydroxy-1,2,3,4-tetrahydro-4,4-dimethyl-7-bromo-naphthalen-1-yl)acetate
المتفاعلات
الكواشف
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةThe resulting mixture was heated for 2 h
- 2أخرىthe solution decanted from the residual solids
- 3غسيلThe solids were washed with EtOAc
- 4غسيلthe combined organic layers were washed with cold 15% H2SO4, saturated aqueous NaHCO3, and saturated aqueous NaCl
- 5تجفيفbefore being dried over MgSO4
- 6أخرىRemoval of the solvents undr reduced pressure and column chromatography (10% EtOAc-hexanes)
الإجراء التجريبي
To a suspension of Zn (1.20 g, 18.4 mmol) in 10 mL benzene at 100° C. was slowly added a solution of ethyl 2-bromoacetate (658.0 mg, 3.94 mmol) and 3,4-dihydro-4,4-dimethyl-7-bromo-naphthalen-1(2H)-one (Compound G, 500.0 mg, 1.97 mmol) in 20.0 mL benzene. The resulting mixture was heated for 2 h, cooled to room temperature, and the solution decanted from the residual solids. The solids were washed with EtOAc and the combined organic layers were washed with cold 15% H2SO4, saturated aqueous NaHCO3, and saturated aqueous NaCl before being dried over MgSO4. Removal of the solvents undr reduced pressure and column chromatography (10% EtOAc-hexanes) afforded the title compound as a yellow oil.