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Hydrochloric Acid → HCID 14533171、化合物

HRID 893541
ノート
印刷プレビュー

反応式

HRID 893541 の反応式
[F:1][C:2]([F:12])([F:11])[CH:3]([CH2:7][CH2:8][CH2:9][CH3:10])[CH2:4][CH2:5][OH:6].[C:13]1([CH3:23])[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1.Cl>N1C=CC=CC=1>[C:13]1([CH3:23])[CH:18]=[CH:17][C:16]([S:19]([O:6][CH2:5][CH2:4][CH:3]([C:2]([F:11])([F:12])[F:1])[CH2:7][CH2:8][CH2:9][CH3:10])(=[O:21])=[O:20])=[CH:15][CH:14]=1
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 313Hydrochloric AcidHCID 73974-Toluenesulfonyl chlorideHCID 14533169HCID 14533169、化合物

生成物 1

HCID 14533171HCID 14533171、化合物収率 92%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

0.48 g of 3-trifluoromethyl-1-heptanol was dissolved in 0.79 g of pyridine, and the solution was cooled with ice, followed by addition of 0.5 g of p-toluenesulfonyl chloride, stirring for 2 hours under cooling with ice and stirring for 2 hours at room temperature. After the reaction, the product was acidified with 2N-hydrochloric acid and extracted with methylene chloride. The resultant methylene chloride solution was washed with water and dried with magnesium sulfate, and the solvent was distilled off, whereby 3-trifluoromethylheptyl p-toluenesulfonate was obtained in an amount of 0.82 g (yield: 92%) and showed: [α]D23 +0.5, [α]D23 +2.2 (c 2, methylene chloride).

後処理

  1. temperaturethe solution was cooled with ice
  2. temperatureunder cooling with ice
  3. stirringstirring for 2 hours at room temperature
  4. customAfter the reaction
  5. extractionextracted with methylene chloride
  6. washThe resultant methylene chloride solution was washed with water
  7. dry with materialdried with magnesium sulfate
  8. distillationthe solvent was distilled off

出典と根拠

ORDレコード
ord-4e5a2d23c85d4ffc93445d69c851bf9c
出典データセット
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05126071

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