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Thionyl Chloride → 4-(4-Chlorobutyl)pyridine

HRID 892460
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HRID 892460 반응식
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9][CH2:10]O)=[CH:3][CH:2]=1.S(Cl)([Cl:14])=O>C(Cl)(Cl)Cl>[N:1]1[CH:6]=[CH:5][C:4]([CH2:7][CH2:8][CH2:9][CH2:10][Cl:14])=[CH:3][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 27846554-Pyridinebutanol

생성물 1

HCID 109539414-(4-Chlorobutyl)pyridine수율 90.4%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

A solution of 4-(4-pyridinyl)-1-butanol (Mayer J. M. and Testa, B., Helv. Chim. Acta 65, pages 1868-1884 (1982)) (4.20 g, 27.7 mmol) in 30 mL of chloroform is cooled to 0° C. and treated with thionyl chloride (6.60 g, 55.54 mmol) in 30 mL of chloroform. The reaction is allowed to warm to room temperature over 15 hours. The volatiles are removed in vacuo. The residue is cooled to 0° C. and treated with 50 mL of cold 10% sodium hydroxide solution and the mixture is extracted with three 100-mL portions of chloroform. The combined organic extracts are dried over sodium sulfate and the solvents are removed under reduced pressure to give 4.25 g of 4-(4-pyridinyl)-1-butylchloride as a brown oil.

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후처리

  1. customThe volatiles are removed in vacuo
  2. temperatureThe residue is cooled to 0° C.
  3. additiontreated with 50 mL of cold 10% sodium hydroxide solution
  4. extractionthe mixture is extracted with three 100-mL portions of chloroform
  5. dry with materialThe combined organic extracts are dried over sodium sulfate
  6. customthe solvents are removed under reduced pressure

출처 및 근거

ORD 기록
ord-92dd2d59e02d41eeaa805db3f77beb89
출처 데이터셋
uspto-grants-1992_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05118691

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