反応 #1494

ord-bf2e44a5bdea4415bef84fd79bdef046

反応方程式

CCOC(=O)CBr
ethyl 2-bromoacetate
CC1(C)CCC(=O)c2cc(Br)ccc21
3,4-dihydro-4,4-dimethyl-7-bromo-naphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
CC1(C)CCC(=O)c2cc(Br)ccc21
Compound G
CC1(C)CCC(=O)c2cc(Br)ccc21
7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one
CCOC(=O)CC1(O)CCC(C)(C)c2ccc(Br)cc21
title compound
CCOC(=O)CC1(O)CCC(C)(C)c2ccc(Br)cc21
(±)Ethyl 2-(1-hydroxy-1,2,3,4-tetrahydro-4,4-dimethyl-7-bromo-naphthalen-1-yl)acetate

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The resulting mixture was heated for 2 h
  2. 2
    その他the solution decanted from the residual solids
  3. 3
    洗浄The solids were washed with EtOAc
  4. 4
    洗浄the combined organic layers were washed with cold 15% H2SO4, saturated aqueous NaHCO3, and saturated aqueous NaCl
  5. 5
    乾燥before being dried over MgSO4
  6. 6
    その他Removal of the solvents undr reduced pressure and column chromatography (10% EtOAc-hexanes)

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723666uspto-grants-1998_03