반응 #2304276

ord-94d203fd3bfe4f7f9eceaaaf3f0fc14c

반응 방정식

C[Si](C)(C)Cl
Trimethylsilyl chloride
O
water
Cc1ccc(Br)cc1O
5-bromo-2-methylphenol
Cc1ccc(Br)cc1O
Intermediate 1
Cc1ccc(Br)cc1O
5-bromo-2-methylphenol
[Li][CH2]CCC
n-butyl lithium
Cc1ccc([Si](C)(C)C)cc1O[Si](C)(C)C
2-methyl-5-(trimethylsilyl)phenoxytrimethylsilane
수율 102.6%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe solution stirred at −78° C. for 1.5 hours
  2. 2
    추출The mixture was extracted with diethyl ether (2×75 mL)
  3. 3
    건조the combined organic extracts were dried (magnesium sulphate)
  4. 4
    농축concentrated under reduced pressure

실험 절차

To a solution of 5-bromo-2-methylphenol (Intermediate 1, 3.6 g, 19.3 mmol) in THF (150 mL) at −78° C. was added n-butyl lithium (30 mL, 1.6 M solution in hexanes, 48.1 mmol) and the reaction stirred at this temperature for 30 minutes. Trimethylsilyl chloride (6.1 mL, 48.1 mmol) was then added and the solution stirred at −78° C. for 1.5 hours. The reaction was allowed to warm to room temperature and water (75 mL) was added. The mixture was extracted with diethyl ether (2×75 mL) and the combined organic extracts were dried (magnesium sulphate) and concentrated under reduced pressure to afford 2-methyl-5-(trimethylsilyl)phenoxytrimethylsilane (5 g) as a yellow oil. 1H NMR δH 0.26 (9 H, s), 0.29 (9 H, s), 2.20 (3 H, s), 6.93 (1 H, d, J=1.1 Hz), 7.04 (1 H, dd, J=7.3, 1.1 Hz), 7.16 (1 H, d, J=7.4 Hz).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07407649B2uspto-grants-2008_08