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Potassium Hydroxide → 2-Amino-1-(4-bromophenyl)-1-ethanol

HRID 1160210
ノート
印刷プレビュー

反応式

HRID 1160210 の反応式
[BH4-].[Na+].[OH-].[K+].Cl.[NH2:6][CH2:7][C:8]([C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=1)=[O:9]>CO>[NH2:6][CH2:7][CH:8]([C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=1)[OH:9]
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 14797Potassium HydroxideHCID 27982162-Amino-1-(4-bromophenyl)ethan-1-one hydrochlorideHCID 4311764Sodium borohydride

生成物 1

HCID 137289422-Amino-1-(4-bromophenyl)-1-ethanol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

実験手順

Sodium borohydride (227 mg, 6.00 mmol) was dissolved in methanol (10 mL) and 5% potassium hydroxide in methanol (4.49 mL, 4.00 mmol) was carefully added. To this solution was added 2-Amino-1-(4-bromo-phenyl)-ethanone hydrochloride (1.0 g, 4.00 mmol) dissolved in methanol (10 mL) and stirring continued for 0.2 hours at room temperature. The mixture was concentrated, and quenched with saturated sodium bicarbonate (10 mL) and extracted with dichloromethane several times. The organics were combined, dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. The title compound was isolated as a yellow solid (677 mg, 77%). 1H NMR (300 MHz, CDCl3): 7.51-7.47 (d. 2H), 7.27-7.23 (d, 2H), 4.63-4.59 (m, 1H), 3.03 (dd, 1H), 2.76 (dd, 1H)

後処理

  1. concentrationThe mixture was concentrated
  2. customquenched with saturated sodium bicarbonate (10 mL)
  3. extractionextracted with dichloromethane several times
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-d6385e3f14544f3fa1a967fe8d8cf8cb
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07816354B2

反応ノート

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