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Benzyl Bromide → HCID 18461312, 화합물

HRID 2303913
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HRID 2303913 반응식
[CH2:1](Br)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[C:15]([O:18][C:19]1[CH:24]=[C:23]([C:25]([CH3:28])([CH3:27])[CH3:26])[C:22]([OH:29])=[CH:21][C:20]=1[C:30]([CH3:33])([CH3:32])[CH3:31])(=[O:17])[CH3:16]>CC(C)=O>[C:15]([O:18][C:19]1[CH:24]=[C:23]([C:25]([CH3:26])([CH3:28])[CH3:27])[C:22]([O:29][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:21][C:20]=1[C:30]([CH3:33])([CH3:32])[CH3:31])(=[O:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 53998699HCID 53998699, 화합물

생성물 1

HCID 18461312HCID 18461312, 화합물수율 68.9%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Benzyl bromide (5.17 g) and potassium carbonate (4.15 g) were added to a solution of 2,5-di-t-butyl-4-hydroxyphenyl acetate (5.3 g) in acetone (40 ml). The mixture was stirred at ambient temperature for 48 hours. The reaction mixture was partitioned between ethyl acetate and water. The ethyl acetate layer was dried over anhydrous sodium sufate and concentrated. The residue was purified by chromatography on a silica gel column using c-hexane/diisopropyl ether=10/1 as the eluant to give the title compound (4.9 g).

후처리

  1. customThe reaction mixture was partitioned between ethyl acetate and water
  2. dry with materialThe ethyl acetate layer was dried over anhydrous sodium sufate
  3. concentrationconcentrated
  4. customThe residue was purified by chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-7f7549e211854708853c0af6a4833741
출처 데이터셋
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06432993B1

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