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Methanesulfonyl chloride → (2S)-1-(4-cyanophenoxy)-3-methane-sulfonyloxypropan-2-ol

HRID 466222
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HRID 466222 반응식
[C:1]([C:3]1[CH:14]=[CH:13][C:6]([O:7][CH2:8][C@H:9]([OH:12])[CH2:10][OH:11])=[CH:5][CH:4]=1)#[N:2].[CH3:15][S:16](Cl)(=[O:18])=[O:17]>N1C=CC=CC=1>[C:1]([C:3]1[CH:14]=[CH:13][C:6]([O:7][CH2:8][C@H:9]([OH:12])[CH2:10][O:11][S:16]([CH3:15])(=[O:18])=[O:17])=[CH:5][CH:4]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 12222186(2R)-3-(4-cyanophenoxy)propane-1,2-diol

생성물 1

HCID 15066864(2S)-1-(4-cyanophenoxy)-3-methane-sulfonyloxypropan-2-ol

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

57.2 g of (2R)-3-(4 cyanophenoxy)propane-1,2-diol was dissolved in dry pyridine, (300 ml) and treated dropwise with methanesulfonyl chloride, (20.7 ml), at -10° C. The reaction mixture was kept at 5° C. overnight, evaporated at reduced pressure and poured on ice and 2 M hydrochloric acid. The solid precipitate was recrystallized three times from methanol to yield 12.3 g of the title compound, m.p. 119°-121° C., [α]D20 +9.7° (c 1.0, CH3OH).

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후처리

  1. customevaporated at reduced pressure
  2. additionpoured on ice and 2 M hydrochloric acid
  3. customThe solid precipitate was recrystallized three times from methanol

출처 및 근거

ORD 기록
ord-1f2068e8415c42a5ac0d8a34e1ff74c8
출처 데이터셋
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05155133

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