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N-Methylcyclohexylamine → N-cyclohexyl-N-methylethenesulfonamide

HRID 1968840
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인쇄 미리보기

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HRID 1968840 반응식
[CH3:1][NH:2][CH:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.Cl[CH2:10][CH2:11][S:12](Cl)(=[O:14])=[O:13]>C(Cl)Cl>[CH:3]1([N:2]([CH3:1])[S:12]([CH:11]=[CH2:10])(=[O:14])=[O:13])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1
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참가 물질

4

반응물 2

HCID 7514N-MethylcyclohexylamineHCID 15385Ethanesulfonylchloride, 2-chloro-

생성물 1

HCID 58625116N-cyclohexyl-N-methylethenesulfonamide

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
5 °C

실험 절차

A mixture of N-methylcyclohexylamine (0.048 mol) and TEA (0.053 mol) in DCM (200 mL) was cooled in an ice bath to 5° C., and then a solution of 2-chloro-ethanesulfonyl chloride (0.048 mol, 97%) in DCM (20 mL) was added dropwise. The reaction mixture was stirred for 2 hours at room temperature and then was washed with H2O. The organic layer was separated, dried (MgSO4), and filtered, and the solvent was evaporated to yield the title compound as a residue.

후처리

  1. washwas washed with H2O
  2. customThe organic layer was separated
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-25fa093c38a5463cab8eb9e624f518b5
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08426429B2

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