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Dichloromethane → HCID 86662056, 화합물

HRID 869257
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인쇄 미리보기

반응식

HRID 869257 반응식
[CH3:1][N:2]([C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)[CH2:3][CH2:4][OH:5].ClCCl.C(N(CC)CC)C.[S:25](Cl)([CH3:28])(=[O:27])=[O:26]>O>[CH3:28][S:25]([O:5][CH2:4][CH2:3][N:2]([CH3:1])[C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([N+:12]([O-:14])=[O:13])[CH:7]=1)(=[O:27])=[O:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 20538799HCID 20538799, 화합물

생성물 1

HCID 86662056HCID 86662056, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a mixture of 2-[methyl(3-nitrophenyl)amino]ethanol (780 mg) and dichloromethane (20 mL), triethylamine (0.66 mL) and mesyl chloride (0.37 mL) were added sequentially under ice cooling and stirred for 3 hours. Water was added to the reaction liquid, and the organic layer was separated and washed with saturated aqueous sodium chloride. After drying over anhydrous magnesium sulfate, the solvent was distilled off to give 2-[methyl(3-nitrophenyl)amino]ethyl methanesulfonate (1.0 g) as a yellow solid.

후처리

  1. additionwere added sequentially under ice cooling
  2. customthe organic layer was separated
  3. washwashed with saturated aqueous sodium chloride
  4. dry with materialAfter drying over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled off

출처 및 근거

ORD 기록
ord-769d024997d94a58bd8085dcbd652ddb
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969336B2

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