Lithium Hydroxide → 5-Bromo-2-(3-tert-butoxycarbonyl-propoxy)-4-chloro-benzoic acid

HRID 448926노트

반응식

HRID 448926 반응식
C(OC(CCC[O:11][C:12](=[O:32])[C:13]1[CH:18]=[C:17]([Br:19])[C:16]([Cl:20])=[CH:15][C:14]=1[O:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])=O)(C)(C)C.[Li+].[OH-].OS([O-])(=O)=O.[Na+]>C1COCC1>[Br:19][C:17]1[C:16]([Cl:20])=[CH:15][C:14]([O:21][CH2:22][CH2:23][CH2:24][C:25]([O:27][C:28]([CH3:30])([CH3:29])[CH3:31])=[O:26])=[C:13]([CH:18]=1)[C:12]([OH:32])=[O:11]

참가 물질

5

반응물 3

HCID 3939Lithium HydroxideHCID 516919Sodium BisulfateHCID 686035915-Bromo-2-(3-tert-butoxycarbonyl-propoxy)-4-chloro-benzoic acid 3-tert-butoxycarbonyl-propyl ester

생성물 1

HCID 686032665-Bromo-2-(3-tert-butoxycarbonyl-propoxy)-4-chloro-benzoic acid수율 41.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 5-bromo-2-(3-tert-butoxycarbonyl-propoxy)-4-chloro-benzoic acid 3-tert-butoxycarbonyl-propyl ester (8.2 g, 15.3 mmol) and LiOH (19.1 mL, 4 N, 76.6 mmol) in THF (150 mL) was stirred at rt for 16 hrs. The mixture was acidified by saturated NaHSO4 (50 mL) and extracted with ethyl acetate. The ethyl acetate layer was dried over Na2SO4, filtered and concentrated. The residue was purified via silica gel flash chromatography (eluting with 50% ethyl acetate in hexane), followed by crystallization in hexane/ethyl acetate (10/1) to afford 5-bromo-2-(3-tert-butoxycarbonyl-propoxy)-4-chloro-benzoic acid as white crystals (2.5 g). MS [M-(iso-butene+OH)]+: 320.8; tR=2.38 min. (method 1)

후처리

  1. extractionextracted with ethyl acetate
  2. dry with materialThe ethyl acetate layer was dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified via silica gel flash chromatography (eluting with 50% ethyl acetate in hexane)
  6. customfollowed by crystallization in hexane/ethyl acetate (10/1)

출처 및 근거

ORD 기록
ord-a81ec6164d6c49c99c01e762ea4fc8ff
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08481738B2

반응 노트

불러오는 중…