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Methanesulfonyl chloride → (S)-3-Fluoroheptyl Methanesulfonate

HRID 1197388
ノート
印刷プレビュー

反応式

HRID 1197388 の反応式
[F:1][C@@H:2]([CH2:6][CH2:7][CH2:8][CH3:9])[CH2:3][CH2:4][OH:5].[CH3:10][S:11](Cl)(=[O:13])=[O:12]>N1C=CC=CC=1>[CH3:10][S:11]([O:5][CH2:4][CH2:3][C@@H:2]([F:1])[CH2:6][CH2:7][CH2:8][CH3:9])(=[O:13])=[O:12]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 31297Methanesulfonyl chlorideHCID 54122660(S)-3-fluoroheptanol

生成物 1

HCID 22850589(S)-3-Fluoroheptyl Methanesulfonate収率 93.18%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a 100 ml flask were added 8.7 g of (S)-3-fluoroheptanol and 21.5 g of pyridine in a nitrogen stream, and the solution was kept at 5° to 10° C. To the solution was added dropwise 7.5 g of methanesulfonyl chloride over 30 minutes, followed by stirring at 15° C. or less for 5 hours. The reaction mixture was poured into 200 ml of ice-water and extracted with ethyl acetate. The organic layer was washed successively with a diluted hydrochloric aqueous solution and water, dried over magnesium sulfate, and freed of the solvent by distillation at 30° C. or lower to obtain 12.7 g (93.18%) of the titled compound.

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

後処理

  1. customwas kept at 5° to 10° C
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed successively with a diluted hydrochloric aqueous solution and water
  4. dry with materialdried over magnesium sulfate
  5. distillationfreed of the solvent by distillation at 30° C.

出典と根拠

ORDレコード
ord-ba8ddb1e94294198babfad6d4ab38a0e
出典データセット
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05275756

反応ノート

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