Hydrochloric Acid → 2-Bromo-4,6-bis(trifluoromethyl)benzaldehyde

HRID 405184

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HRID 405184 반응식
[Li]CCCC.CC1(C)CCCC(C)(C)N1.[Br:16][C:17]1[CH:22]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:20]=[C:19]([C:27]([F:30])([F:29])[F:28])[CH:18]=1.[CH:31](OCC)=[O:32].Cl>C1COCC1>[Br:16][C:17]1[CH:22]=[C:21]([C:23]([F:24])([F:25])[F:26])[CH:20]=[C:19]([C:27]([F:28])([F:29])[F:30])[C:18]=1[CH:31]=[O:32]

참가 물질

7

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온도
-78 °C

실험 절차

A 2.59 M hexanes solution of n-BuLi (1.13 mL, 2.92 mmol) was added dropwise to a, 0° C., THF solution (4 mL) of 2,2,6,6-tetramethylpiperidine (0.50 mL, 2.92 mmol). After 5 min at 0° C., the solution was cooled to −78° C. and 1-bromo-3,5-bis(trifluoromethyl)benzene was added dropwise over 2 min. The resulting brown amber colored solution was stirred at −78° C. for an additional 20 min. Ethyl formate (0.587 mL, 7.30 mmol) was then added dropwise at −78° C. over 1 min. After 30 min at −78° C., 1 M aqueous HCl was added, the layers were separated and the organic layer was washed with 0.1 M aqueous HCl and 1 M aqueous. The organic layer was dried (Na2SO4), concentrated, and short path vacuum distilled to provide the title compound.

후처리

  1. waitAfter 30 min at −78° C.
  2. customthe layers were separated
  3. washthe organic layer was washed with 0.1 M aqueous HCl and 1 M aqueous
  4. dry with materialThe organic layer was dried (Na2SO4)
  5. concentrationconcentrated
  6. distillationshort path vacuum distilled

출처 및 근거

ORD 기록
ord-9e6e1e238479481e94e033818886ccae
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08748624B2

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