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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → 6-Chloroundecane

HRID 23801
ノート
印刷プレビュー

反応式

HRID 23801 の反応式
CS(O[CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11])(=O)=O.[Cl-:17].[Li+].O>CN(C)C=O>[Cl:17][CH:6]([CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]
参加物反応条件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 962WaterHCID 433294Lithium ChlorideHCID 225905206-Methanesulfonyloxyundecane

生成物 1

HCID 99206036-Chloroundecane収率 97.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
15 °C

実験手順

Thirty grams (0.12 mol) of 6-methanesulfonyloxyundecane was dissolved in 150 mL of N,N-dimethylformamide and 15.3 g (0.36 mol) of anhydrous lithium chloride was added to the solution under cooling with ice. The mixture was warmed to 50˜55° C. and stirred for 3 hours. Thereafter, the mixture was cooled to 15° C. and 300 mL of cold water was added. The reaction mixture was extracted three times with 150 mL of hexane and the organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride and thereafter dried over 6 g of anhydrous magnesium sulfate. After filtering off the anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure to give 22.2 g (97.1% in yield) of 6-chloroundecane.

後処理

  1. temperatureunder cooling with ice
  2. temperatureThe mixture was warmed to 50˜55° C.
  3. extractionThe reaction mixture was extracted three times with 150 mL of hexane
  4. washthe organic layer was sequentially washed with 150 mL of water and 150 mL of a saturated aqueous solution of sodium chloride
  5. dry with materialdried over 6 g of anhydrous magnesium sulfate
  6. filtrationAfter filtering off the anhydrous magnesium sulfate
  7. distillationthe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-552f94c5b02243eb9ca1115a3c9d097d
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06852867B2

反応ノート

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