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Water → 6-Chloroundecane

HRID 23801
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HRID 23801 반응식
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]
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참가 물질

5

반응물 3

HCID 962WaterHCID 433294Lithium ChlorideHCID 225905206-Methanesulfonyloxyundecane

생성물 1

HCID 99206036-Chloroundecane수율 97.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
15 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-552f94c5b02243eb9ca1115a3c9d097d
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06852867B2

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