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Sodium Hydroxide → N-(4-Chloro-3-hydroxymethyl-benzyl)-propionamide

HRID 2428131
ノート
印刷プレビュー

反応式

HRID 2428131 の反応式
[OH-].[Na+].C([SiH2][O:8][C:9](C)(C)[C:10]1[CH:11]=[C:12]([CH:19]=[CH:20][C:21]=1[Cl:22])[CH2:13][NH:14][C:15](=[O:18])[CH2:16][CH3:17])(C)(C)C>CO>[Cl:22][C:21]1[CH:20]=[CH:19][C:12]([CH2:13][NH:14][C:15](=[O:18])[CH2:16][CH3:17])=[CH:11][C:10]=1[CH2:9][OH: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

4

反応物 2

HCID 14798Sodium HydroxideHCID 137328720N-[3-(tert-Butyl-dimethyl-silanyloxymethyl)-4-chloro-benzyl]-propionamide

生成物 1

HCID 67148202N-(4-Chloro-3-hydroxymethyl-benzyl)-propionamide収率 88.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

Aq. 1M NaOH (92 mL) was added to a sol. of N-[3-(tert-butyl-dimethyl-silanyloxymethyl)-4-chloro-benzyl]-propionamide (5.08 g, 14.9 mmol) in MeOH (184 mL). The mixture was heated to 80° C., and stirred at this temperature for 30 min. The mixture was allowed to cool to rt, and the solvents were partially removed under reduced pressure. The aq. residue was diluted with water, and was extracted with EtOAc (3×). The combined org. extracts were washed with brine, dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Purification of the crude by FC(CH2Cl2→MeOH/CH2Cl2 1:9) yielded the title compound (2.99 g, 88%). LC-MS: tR=0.67 min; ES+: 269.31.

後処理

  1. temperatureto cool to rt
  2. customthe solvents were partially removed under reduced pressure
  3. additionThe aq. residue was diluted with water
  4. extractionwas extracted with EtOAc (3×)
  5. washextracts were washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. customthe solvents were removed under reduced pressure
  9. customPurification of the crude by FC(CH2Cl2→MeOH/CH2Cl2 1:9)

出典と根拠

ORDレコード
ord-45e2b84b342d4108a4e637e27842659f
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07968720B2

反応ノート

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