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Benzyl Bromide → HCID 18461312、化合物

HRID 2303913
ノート
印刷プレビュー

反応式

HRID 2303913 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7498Benzyl BromideHCID 11430Potassium CarbonateHCID 53998699HCID 53998699、化合物

生成物 1

HCID 18461312HCID 18461312、化合物収率 68.9%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-7f7549e211854708853c0af6a4833741
出典データセット
uspto-grants-2002_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06432993B1

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート