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Hydrochloric Acid → (S)-6-(Hydroxymethyl)morpholin-3-one

HRID 2262473
ノート
印刷プレビュー

反応式

HRID 2262473 の反応式
CC([O-])(C)C.[K+].Cl[CH2:8][C:9]([NH:11][CH2:12][C@H:13]([OH:16])[CH2:14][OH:15])=[O:10].CO.Cl>O>[OH:15][CH2:14][C@@H:13]1[CH2:12][NH:11][C:9](=[O:10])[CH2:8][O:16]1
参加物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 313Hydrochloric AcidHCID 887MethanolHCID 11378718(S)-2-Chloro-N-(2,3-dihydroxypropyl)acetamideHCID 23665647Potassium tert-butoxide

生成物 1

HCID 11446350(S)-6-(Hydroxymethyl)morpholin-3-one収率 20.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of t-BuOK (13.7 g, 122 mmol) in t-AmOH (175 mL) was added a solution of 2-chloro-N—[(S)-2,3-dihydroxypropyl]acetamide (8.1 g, 48.3 mmol) in t-AmOH (325 mL) at room temperature over 2 h. The resulting suspension was stirred for 1 h at room temperature. Methanol (50 mL) and water (5 mL) were added and the resulting solution was stirred for 0.5 h at room temperature before adjusting the pH to 5 by the addition of conc. HCl. The suspension was filtered and the solid washed with methanol. The filtrate was evaporated in vacuo, the resulting solid was slurried in methanol (50 mL) and filtered off to afford (S)-6-(hydroxymethyl)morpholin-3-one (1.3 g) as a white solid. A second crop was obtained by adding EtOAc (200 mL) to the filtrate and filtering the resulting solution through a silica plug (1×10 cm). The solvent was evaporated in vacuo to afford (S)-6-(hydroxymethyl)morpholin-3-one (3.9 g, overall yield 5.2 g, 82%) as a white solid.

後処理

  1. stirringthe resulting solution was stirred for 0.5 h at room temperature
  2. filtrationThe suspension was filtered
  3. washthe solid washed with methanol
  4. customThe filtrate was evaporated in vacuo
  5. filtrationfiltered off

出典と根拠

ORDレコード
ord-87e4e95fd9e2460783eac0864fd0bc10
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07851471B2

反応ノート

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