홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Triethylamine → (2S)-2-methoxypropyl 4-methylbenzene-1-sulfonate

HRID 339085
노트
인쇄 미리보기

반응식

HRID 339085 반응식
[CH3:1][O:2][C@@H:3]([CH3:6])[CH2:4][OH:5].[CH3:7]CN(CC)CC.[C:14]1(C)[C:15]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:17]=[CH:18][CH:19]=1>C(Cl)Cl>[CH3:7][C:18]1[CH:19]=[CH:14][C:15]([S:20]([O:5][CH2:4][C@@H:3]([O:2][CH3:1])[CH3:6])(=[O:21])=[O:22])=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 8623o-Toluenesulfonyl chlorideHCID 6424022-Methoxy-1-propanol, (2S)-

생성물 1

HCID 13896528(2S)-2-methoxypropyl 4-methylbenzene-1-sulfonate수율 75%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a stirred solution of (S)-2-methoxypropan-1-ol (1.00 g, 11.1 mmol) in DCM (50 mL) was added Et3N (2.33 mL, 16.6 mmol). A solution of toluene sulfonyl chloride (2.54 g, 13.3 mmol) in DCM (20 mL) was added dropwise at 0° C. under nitrogen. The reaction mixture was allowed to warm to ambient temperature and was stirred overnight. The reaction was diluted with DCM, washed with saturated aqueous NaHCO3 and brine, dried and concentrated. The residue was purified by flash chromatography on silica gel (hexanes:EtOAc, 10:1 to 4:1) to give (S)-2-methoxypropyl 4-methylbenzenesulfonate (2.03 g, 75%).

후처리

  1. washwashed with saturated aqueous NaHCO3 and brine
  2. customdried
  3. concentrationconcentrated
  4. customThe residue was purified by flash chromatography on silica gel (hexanes:EtOAc, 10:1 to 4:1)

출처 및 근거

ORD 기록
ord-3296c8bcd47a48269f7dd2b662c9a625
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889704B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트