반응 #1470

ord-becf0ee7c3024fadba4ea32c31403111

반응 방정식

CC1(C)CCC(=O)c2cc(Br)ccc21
4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-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
C1CCOC1
THF
Sc1ccccc1
thiophenol
CCN(CC)CC
triethylamine
C1CCOC1
THF
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
title compound
CC1(C)CC=C(Sc2ccccc2)c2cc(Br)ccc21
4.4-Dimethyl-7-bromo-1-phenylthio-3,4-dihydronaphthalene

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with ether (3×50 mL)
  2. 2
    세척The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL)
  3. 3
    건조The organic layer was dried (MgSO4)
  4. 4
    workup.DISTILLATIONthe solvent distilled off at reduced pressure

실험 절차

To a stirred solution of 4,4-dimethyl-7-bromo-3,4-dihydronaphthalen-1(2H)one (Compound G, 1.48 g, 5.9 mmol), titanium tetrachloride (1.09 g, 5.7 mmol) and THF (10 mL) was added a mixture of thiophenol (660 mg, 6 mmol), triethylamine (1.16 g, 11.5 mmol) and THF (20 mL) via an addition funnel at ambient temperature. The mixture was stirred for 5 h, and water (10 mL) was added, extracted with ether (3×50 mL). The combined organic layer was washed successively with water (10 mL), 10% NaHCO3 (10 mL) and brine (10 mL). The organic layer was dried (MgSO4) and the solvent distilled off at reduced pressure. After silicagel chromatography the title compound was obtained as a colorless oil.

출처

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