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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Toluenesulfonyl chloride → 2-(2-Ethoxyethoxy)ethyl 4-methylbenzene-1-sulfonate

HRID 1167667
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HRID 1167667 반응식
[CH2:1]([O:3][CH2:4][CH2:5][O:6][CH2:7][CH2:8][OH:9])[CH3:2].C(N(CC)CC)C.[C:17]1([CH3:27])[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1>ClCCl>[CH3:27][C:17]1[CH:22]=[CH:21][C:20]([S:23]([O:9][CH2:8][CH2:7][O:6][CH2:5][CH2:4][O:3][CH2:1][CH3:2])(=[O:25])=[O:24])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 73974-Toluenesulfonyl chlorideHCID 8146Diethylene Glycol Monoethyl EtherHCID 8471Triethylamine

생성물 1

HCID 41182322-(2-Ethoxyethoxy)ethyl 4-methylbenzene-1-sulfonate수율 82%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

432 mg (3.22 mmol) of 2-(2-ethoxyethoxy)ethanol was dissolved in 40 ml of dichloromethane, and 0.6 ml (4.19 mmol) of triethylamine and 614 mg (3.22 mmol) of p-toluenesulfonyl chloride were added thereto. The mixture was stirred at room temperature for 15 hours. After the solvent was removed under reduced pressure, 40 ml of water was added thereto. The mixture was extracted with 30 ml of ethyl acetate. The solvent was removed under reduced pressure to give 760 mg (2.64 mmol) of the title compound in a yield of 82%.

후처리

  1. customAfter the solvent was removed under reduced pressure, 40 ml of water
  2. additionwas added
  3. extractionThe mixture was extracted with 30 ml of ethyl acetate
  4. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-394e249e55cc4633b205701916b87025
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06620831B2

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