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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium hydrosulfide hydrate → Sodium 2-hydroxy-3-sulfanylpropane-1-sulfonate

HRID 1275416
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HRID 1275416 반응식
O.Cl[CH2:3][CH:4]([OH:10])[CH2:5][S:6]([O-:9])(=[O:8])=[O:7].[Na+:11].O.[SH-:13].[Na+]>CN(C=O)C>[SH:13][CH2:3][CH:4]([OH:10])[CH2:5][S:6]([O-:9])(=[O:8])=[O:7].[Na+:11]
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참가 물질

4

반응물 2

HCID 16211346Sodium hydrosulfide hydrateHCID 23665651Sodium 3-chloro-2-hydroxypropane-1-sulfonate--water (1/1/1)

생성물 1

HCID 23663670Sodium 2-hydroxy-3-sulfanylpropane-1-sulfonate수율 172.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To sodium 3-chloro-2-hydroxypropanesulfonate hydrate (2.0 g), sodium hydrosulfide hydrate (0.42 g) was added in 10 mL DMF. The mixture was refluxed overnight. When the reaction mixture was cooled down, white solid was isolated, rinsed with ether and acetone to obtain 1.9 g crude sodium 3-mercapto-2-hydroxypropane sulfonate. The crude product was dissolved in water and preferentially precipitated the desired product by adding acetone. The precipitated product was then filtered and dried under vacuum to get 1.04 g of the title compound.

후처리

  1. temperatureThe mixture was refluxed overnight
  2. temperatureWhen the reaction mixture was cooled down
  3. customwhite solid was isolated
  4. washrinsed with ether and acetone

출처 및 근거

ORD 기록
ord-dba88060dfeb4f4c8d98aa631c8a672c
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06160167

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