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4-Toluenesulfonyl chloride → HCID 59526126, 화합물

HRID 385883
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HRID 385883 반응식
[OH:1][CH2:2][CH2:3][NH:4][CH2:5][C@H:6]([OH:8])[CH3:7].CCN([CH2:14][CH3:15])CC.[S:16](Cl)([C:19]1[CH:25]=[CH:24][C:22]([CH3:23])=[CH:21][CH:20]=1)(=[O:18])=[O:17]>C(Cl)Cl>[OH:8][C@H:6]([CH3:7])[CH2:5][N:4]([S:16]([C:19]1[CH:25]=[CH:24][C:14]([CH3:15])=[CH:21][CH:20]=1)(=[O:18])=[O:17])[CH2:3][CH2:2][O:1][S:16]([C:19]1[CH:25]=[CH:24][C:22]([CH3:23])=[CH:21][CH:20]=1)(=[O:18])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 38988844(2r)-1-[(2-Hydroxyethyl)amino]propan-2-ol

생성물 1

HCID 59526126HCID 59526126, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (2R)-1-[(2-hydroxyethyl)amino]propan-2-ol (130.0 g, 1.09 mol) in CH2Cl2 (2 L) and Et3N (304 mL, 2.18 mol) was added TsCl (305 g, 1.60 mol) portion-wise at 0° C. The mixture was maintained at room temperature overnight, then washed with water (800 mL) and brine (500 mL), dried over Na2SO4, filtered and concentrated in vacuo. The resulting residue was purified by silica gel chromatography, eluting with ethyl acetate/petroleum ether to give the title compound as a white solid.

후처리

  1. washwashed with water (800 mL) and brine (500 mL)
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customThe resulting residue was purified by silica gel chromatography
  6. washeluting with ethyl acetate/petroleum ether

출처 및 근거

ORD 기록
ord-a1d83dfff5474bd498850bc0299db302
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367706B2

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