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Methanol → Methyl (2R,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride

HRID 1184567
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HRID 1184567 반응식
Cl.[OH:2][C@@H:3]1[CH2:7][NH:6][C@@H:5]([C:8]([OH:10])=[O:9])[CH2:4]1.S(Cl)([Cl:13])=O.[CH3:15]O>>[ClH:13].[OH:2][C@@H:3]1[CH2:7][NH:6][C@@H:5]([C:8]([O:10][CH3:15])=[O:9])[CH2:4]1
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참가 물질

4

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 44890824(2R,4S)-4-hydroxypyrrolidine-2-carboxylic acid hydrochloride

생성물 1

HCID 44118802Methyl (2R,4S)-4-hydroxypyrrolidine-2-carboxylate hydrochloride

반응 조건

온도
22.5 °C

실험 절차

To a suspension of trans-4-hydroxy-D-proline hydrochloride (150 g, 0.89 mol, 1 equivalent) in methanol (1.25 L), thionyl chloride (130 mL, 1.79 mol, 2 equivalents) was added drop-wise at 0-5° C. Then the reaction mixture was stirred for 4 hours at 20-25° C. The reaction mixture was concentrated under reduced pressure. This crude material was stirred in a mixture of ethanol-methyl tert-butyl ether (1:4, 750 mL) for 30 minutes and the solid was collected by filtration. The wet cake was dried in a vacuum tray dryer for 8 hours at about 50° C. to afford the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 2.03-2.23 (m, 2H), 3.06 (d, 1H, J=12.0 Hz), 3.37 (dd, 2H, J=4.5 Hz, J=12.0 Hz), 3.75 (s, 3H), 4.41-4.48 (m, 2H), 5.64 (bs, 1H), 9.43 (bs, 1H), 10.48 (bs, 1H).

후처리

  1. additionwas added drop-wise at 0-5° C
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. stirringThis crude material was stirred in a mixture of ethanol-methyl tert-butyl ether (1:4, 750 mL) for 30 minutes
  4. filtrationthe solid was collected by filtration
  5. customThe wet cake was dried in a vacuum tray dryer for 8 hours at about 50° C.

출처 및 근거

ORD 기록
ord-a94ca20f617142f39a1653fbcb35948a
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08669255B2

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