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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-(Methylamino)ethanol → 4-Formyl-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide

HRID 874828
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HRID 874828 반응식
[CH3:1][NH:2][CH2:3][CH2:4][OH:5].C(N(CC)CC)C.[CH:13]([C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1)=[O:14]>C(Cl)Cl>[CH:13]([C:15]1[CH:16]=[CH:17][C:18]([S:21]([N:2]([CH2:3][CH2:4][OH:5])[CH3:1])(=[O:23])=[O:22])=[CH:19][CH:20]=1)=[O:14]
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참가 물질

5

반응물 3

HCID 80162-(Methylamino)ethanolHCID 8471TriethylamineHCID 27592104-Formylbenzene-1-sulfonyl chloride

생성물 1

HCID 867223174-Formyl-N-(2-hydroxyethyl)-N-methylbenzenesulfonamide수율 92.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

To an ice-cooled solution of 2-(methylamino)ethanol (0.196 mL, 2.44 mmol) and triethylamine (0.407 mL, 2.93 mmol) in DCM (10 mL) was added 4-formylbenzenesulfonyl chloride (0.500 g, 2.44 mmol). The reaction mixture was warmed slowly to RT and stirred at RT for 80 hours. The reaction mixture was diluted with DCM and was washed with 10% aqueous potassium hydrogen sulfate and dried (magnesium sulfate). The mixture filtered and the solvent evaporated at reduced pressure to afford the title compound (0.548 g, 92%).

후처리

  1. washwas washed with 10% aqueous potassium hydrogen sulfate
  2. dry with materialdried (magnesium sulfate)
  3. filtrationThe mixture filtered
  4. customthe solvent evaporated at reduced pressure

출처 및 근거

ORD 기록
ord-196c8d035891413eac0aea5ba63f1740
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08980913B2

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