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Water → (S)-(+)-1-Acetoxy-3-bromo-2-methyl-propane

HRID 219705
ノート
印刷プレビュー

反応式

HRID 219705 の反応式
[Br:1][CH2:2][C@@H:3]([CH3:6])[CH2:4][OH:5].[C:7](OC(=O)C)(=[O:9])[CH3:8].O.C(OCC)(=O)C>N1C=CC=CC=1>[C:7]([O:5][CH2:4][C@H:3]([CH3:6])[CH2:2][Br:1])(=[O:9])[CH3:8]
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

6

反応物 4

HCID 962WaterHCID 7918Acetic AnhydrideHCID 8857Ethyl AcetateHCID 10986449(S)-(+)-3-Bromo-2-methyl-1-propanol

生成物 1

HCID 10465240(S)-(+)-1-Acetoxy-3-bromo-2-methyl-propane収率 68.3%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
70 °C

実験手順

5 g of (S)-(+)-3-bromo-2-methyl-1-propanol (32.6 mmol) were stirred in 5 ml of pyridine at room temperature. 3.67 g of acetic anhydride (35.9 mmol) were added and the reaction mixture was stirred for 3 h at 70° C. Stirring was continued for 16 h at room temperature. 30 ml of water and 40 ml of ethyl acetate were added. The organic layer was separated and washed with a further portion of water, then dried over magnesium sulfate, filtered, and evaporated under reduced pressure, whereby 4.34 g of the title compound were obtained.

後処理

  1. stirringStirring
  2. waitwas continued for 16 h at room temperature
  3. customThe organic layer was separated
  4. washwashed with a further portion of water
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-11aa72148de94870880eb1a437376a8e
出典データセット
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08202868B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート