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

HRID 355951
ノート
印刷プレビュー

反応式

HRID 355951 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-74d4ccf56cbb483da4bd892d65a2305a
出典データセット
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05834476

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート