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

HRID 2262473
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HRID 2262473 반응식
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
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11378718(S)-2-Chloro-N-(2,3-dihydroxypropyl)acetamideHCID 23665647Potassium tert-butoxide

생성물 1

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

시약·촉매·용매 1

HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-87e4e95fd9e2460783eac0864fd0bc10
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07851471B2

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