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Water → 2-(Cyclohex-2-enyloxy)ethyl 4-methylbenzenesulfonate

HRID 2403750
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인쇄 미리보기

반응식

HRID 2403750 반응식
[CH:1]1([O:7][CH2:8][CH2:9][OH:10])[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.[S:11](Cl)([C:14]1[CH:20]=[CH:19][C:17]([CH3:18])=[CH:16][CH:15]=1)(=[O:13])=[O:12].O>N1C=CC=CC=1>[CH:1]1([O:7][CH2:8][CH2:9][O:10][S:11]([C:14]2[CH:20]=[CH:19][C:17]([CH3:18])=[CH:16][CH:15]=2)(=[O:13])=[O:12])[CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 112865262-(Cyclohex-2-enyloxy)ethanol

생성물 1

HCID 576846852-(Cyclohex-2-enyloxy)ethyl 4-methylbenzenesulfonate

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

To 2-(cyclohex-2-enyloxy)ethanol (intermediate BU) (0.3 g) in anhydrous pyridine was added TsCl (1.3 eq). The mixture was stirred at room temperature for 16 h, after which TLC showed the reaction was complete. The mixture was poured into water, extracted with EA, washed with water and brine, and dried with anhydrous Na2SO4. Solvent was removed and the residue purified by column chromatography to obtain intermediate BV (0.3 g).

후처리

  1. extractionextracted with EA
  2. washwashed with water and brine
  3. dry with materialdried with anhydrous Na2SO4
  4. customSolvent was removed
  5. customthe residue purified by column chromatography
  6. customto obtain intermediate BV (0.3 g)

출처 및 근거

ORD 기록
ord-ad7c48dd05ac4e57b08ac2fe1774defc
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802637B2

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