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Isobutanol → 4-Bromo-2-(2-methylpropoxy)benzoic acid

HRID 2220407
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HRID 2220407 반응식
[H-].[Na+].[CH3:3][CH:4]([CH3:7])[CH2:5][OH:6].[Br:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[C:11](F)[CH:10]=1>CN(C)C=O>[Br:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=[O:14])=[C:11]([O:6][CH2:5][CH:4]([CH3:7])[CH3:3])[CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6560IsobutanolHCID 24758Sodium hydrideHCID 3026814-Bromo-2-fluorobenzoic acid

생성물 1

HCID 248246454-Bromo-2-(2-methylpropoxy)benzoic acid

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a suspension of sodium hydride (60% w/w, 20.5 g) in N,N-dimethylformamide (365 ml) was added 2-methyl-1-propanol (48.7 ml) dropwise below 30° C. over 2 hours under nitrogen atmosphere. To the mixture was added 4-bromo-2-fluorobenzoic acid (50.0 g) slowly below 35° C. To the reaction mixture was added N,N-dimethylformamide (600 ml) and the mixture was stirred at room temperature for 4 days. The reaction mixture was partitioned between water (2000 ml) and hexane (1000 ml). The water layer was separated and acidified with 37% hydrochloric acid. The precipitate was collected by filtration, washed with water and dried at 55° C. to give 4-bromo-2-isobutoxybenzoic acid (62.4 g) as a white solid.

후처리

  1. customThe reaction mixture was partitioned between water (2000 ml) and hexane (1000 ml)
  2. customThe water layer was separated
  3. filtrationThe precipitate was collected by filtration
  4. washwashed with water
  5. customdried at 55° C.

출처 및 근거

ORD 기록
ord-d24519aaa6464469aff2a413ad942d50
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07417060B2

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