Ethanolamine → 2-(4-Chloro-benzylamino)-ethanol

HRID 408588

反応式

HRID 408588 の反応式
[CH2:1]([CH2:3][NH2:4])[OH:2].C([O-])(O)=O.[Na+].[Cl:10][C:11]1[CH:18]=[CH:17][C:14]([CH:15]=O)=[CH:13][CH:12]=1.[BH4-].[Na+]>C1COCC1.CO>[Cl:10][C:11]1[CH:18]=[CH:17][C:14]([CH2:15][NH:4][CH2:3][CH2:1][OH:2])=[CH:13][CH:12]=1

参加物

7

反応条件

温度
0 °C

実験手順

To a solution of ethanolamine (1.2 eq.) in either MeOH or THF were added NaHCO3 (1.5 eq.) and 4-chlorobenzaldehyde (1 eq.). The reaction was refluxed for 4 h, then cooled to 0° C. NaBH4 (1.2 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C., then 15 h at 20° C. The crude was concentrated under reduced pressure then partitioned between water and DCM. The aqueous layer was then extracted twice with DCM. The organic layers were combined, dried over MgSO4, filtered and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with DCM/MeOH: 1/0 to 95/5) to afford 2-(4-chloro-benzylamino)-ethanol.

後処理

  1. temperatureThe reaction was refluxed for 4 h
  2. custom15 h
  3. customat 20° C
  4. concentrationThe crude was concentrated under reduced pressure
  5. customthen partitioned between water and DCM
  6. extractionThe aqueous layer was then extracted twice with DCM
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe crude was purified by chromatography on silica gel (elution with DCM/MeOH: 1/0 to 95/5)

出典と根拠

ORDレコード
ord-bc4addb90c7f49ce91f792e1b8b06d90
出典データセット
uspto-grants-2014_06
特許番号
US08759334B2

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