反応 #1471

ord-afbd95ad9dd44e7e978ad560efb01622

反応方程式

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
CCS
ethanethiol
CCN(CC)CC
triethylamine
CCSC1=CCC(C)(C)c2ccc(Br)cc21
title compound
CCSC1=CCC(C)(C)c2ccc(Br)cc21
2-Bromo-5,6-dihydro-5,5-dimethyl-8-(ethylthio)-naphthalene

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGthe reaction stirred at room temperature for 13 h
  2. 2
    抽出extracted with ether (2×)
  3. 3
    洗浄The organic phase was washed with brine
  4. 4
    乾燥dried over Na2SO4
  5. 5
    濃縮concentrated in vacuo
  6. 6
    その他Purification by flash chromatography (silica, 100% hexane)

実験手順

To a solution of 1.03 g (4.1 mmol) of 7-bromo-3,4-dihydro-4,4-dimethylnaphthalen-1(2H)-one (Compound G) in 30.0 mL of tetrahydrofuran, was added dropwise 0.49 g (0.85 mL, 7.8 mmol) of titaniumtetrachloride and the resulting solution stirred for 10 min. A solution of 35 mg (0.50 mL, 6.7 mmol) of ethanethiol and 0.54 g (0.75 mL, 5.4 mmol) of triethylamine in 10.0 mL of tetrahydrofuran was added and the reaction stirred at room temperature for 13 h. The mixture was diluted with water and extracted with ether (2×). The organic phase was washed with brine, dried over Na2SO4 and then concentrated in vacuo. Purification by flash chromatography (silica, 100% hexane) gave the title compound as an off.

出典

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