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Methanesulfonyl chloride → ethyl (2S)-2-methylsulfonyloxypropanoate

HRID 1722483
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HRID 1722483 반응식
[C:1]([O:6][CH2:7][CH3:8])(=[O:5])[C@H:2]([CH3:4])[OH:3].[CH3:9][S:10](Cl)(=[O:12])=[O:11]>C(N(CC)CC)C>[CH2:7]([O:6][C:1](=[O:5])[C@@H:2]([O:3][S:10]([CH3:9])(=[O:12])=[O:11])[CH3:4])[CH3:8]
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참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 92831(L)-ethyl lactate

생성물 1

HCID 6364515ethyl (2S)-2-methylsulfonyloxypropanoate

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

An equal molar solution of (S)-ethyl lactate and triethylamine in dry methylene was treated with an equal molar amount of methane sulfonylchloride at 5°-10° C. After the addition was complete, the mixture was filtered to remove triethylamine hydrochloride. The filtrate was then washed with water, dried over MgSO4, and concentrated to give a high yield of ethyl-(S)-2[(methylsulfonyl)oxy]propionate.

후처리

  1. additionAfter the addition
  2. filtrationthe mixture was filtered
  3. customto remove triethylamine hydrochloride
  4. washThe filtrate was then washed with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-e8d93e9e3636409594f61ba603ea88f8
출처 데이터셋
uspto-grants-1989_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04855455

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