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Pyridine → 3-(2-Fluorophenyl)propyl 4-methylbenzenesulfonate

HRID 355951
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인쇄 미리보기

반응식

HRID 355951 반응식
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][CH2:10][OH:11].N1C=CC=CC=1.[C:18]1([CH3:28])[CH:23]=[CH:22][C:21]([S:24](Cl)(=[O:26])=[O:25])=[CH:20][CH:19]=1>CCOCC>[S:24]([C:21]1[CH:22]=[CH:23][C:18]([CH3:28])=[CH:19][CH:20]=1)([O:11][CH2:10][CH2:9][CH2:8][C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[F:1])(=[O:26])=[O:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 126185173-(2-Fluorophenyl)propan-1-ol

생성물 1

HCID 224494783-(2-Fluorophenyl)propyl 4-methylbenzenesulfonate

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

17.75 gm of the compound prepared in (3) above was dissolved into 200 ml of dry pyridine. To this was slowly added 24.25 gm of p-toluenesulfonyl chloride at 0° C. and the mixture was stirred for 3 hours at room temperature. After the addition of 300 ml of ether, the mixture was washed with water, followed by the addition of 6N hydrochloric acid to acidify it and washing with saturated brine. The product was dried over anhydrous sodium sulfate and the solvent was evaporated to obtain 31.3 gm of the title compound.

후처리

  1. customat 0° C.
  2. washthe mixture was washed with water
  3. additionfollowed by the addition of 6N hydrochloric acid
  4. washwashing with saturated brine
  5. dry with materialThe product was dried over anhydrous sodium sulfate
  6. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-74d4ccf56cbb483da4bd892d65a2305a
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05834476

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