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Sodium Acetate → Methyl 3-(acetoxymethyl)-4-bromobenzoate

HRID 336265
ノート
印刷プレビュー

反応式

HRID 336265 の反応式
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[CH2:12]Br.[C:14]([O-:17])(=[O:16])[CH3:15].[Na+]>CC(O)=O>[C:14]([O:17][CH2:12][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][C:2]=1[Br:1])[C:6]([O:8][CH3:9])=[O:7])(=[O:16])[CH3:15]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 517045Sodium AcetateHCID 11460987Methyl 4-Bromo-3-(bromomethyl)benzoate

生成物 1

HCID 22574808Methyl 3-(acetoxymethyl)-4-bromobenzoate収率 79.3%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
100 °C

実験手順

To a solution of methyl 4-bromo-3-(bromomethyl)benzoate (6.5 g; 21 mmol; 1 eq.) in AcOH (32.5 mL) was added sodium acetate (3.46 g; 42 mmol; 2 eq.) and the reaction mixture was stirred at 100° C. for 12 hours. After concentration in vacuo, the residue was partitioned between Ethyl acetate and water. The organic layer was washed with 5% aq. NaHCO3 then brine, dried over MgSO4 and concentrated in vacuo. Purification by column chromatography (c-hexane/ethyl acetate, 5/1) afforded the title compound (4.78 g, 79%) as a white solid.

後処理

  1. concentrationAfter concentration in vacuo
  2. customthe residue was partitioned between Ethyl acetate and water
  3. washThe organic layer was washed with 5% aq. NaHCO3
  4. dry with materialbrine, dried over MgSO4
  5. concentrationconcentrated in vacuo
  6. customPurification by column chromatography (c-hexane/ethyl acetate, 5/1)

出典と根拠

ORDレコード
ord-8c27edfddc83460b8315bcb201c8b03f
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889668B2

反応ノート

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