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4-Toluenesulfonyl chloride → HCID 561724, 화합물

HRID 1981562
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인쇄 미리보기

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HRID 1981562 반응식
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][OH:8].[C:9]1([CH3:19])[CH:14]=[CH:13][C:12]([S:15](Cl)(=[O:17])=[O:16])=[CH:11][CH:10]=1>N1C=CC=CC=1>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][O:8][S:15]([C:12]1[CH:13]=[CH:14][C:9]([CH3:19])=[CH:10][CH:11]=1)(=[O:17])=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 73974-Toluenesulfonyl chlorideHCID 748286-Chloro-1-hexanol

생성물 1

HCID 561724HCID 561724, 화합물수율 99%

시약·촉매·용매 1

HCID 1049Pyridine용매

반응 조건

온도
10 °C

실험 절차

A solution of 6-chloro-1-hexanol (100 g) in dry pyridine (500 ml) was treated with p-toluenesulfonyl chloride (227 g) at 5°-10° C. After stirring 2 h at 10° C., the mixture was poured into ice water (2 L), followed by extraction with ethyl ether. The organic extract was washed with ice water and brine, dried, filtered and evaporated to give a syrup, which was further dried at high vacuum. The crude product was overlayered with pentane and cooled in dry ice/acetone to give a solid (210 g, 99%), mp 36°-37° C.

후처리

  1. extractionfollowed by extraction with ethyl ether
  2. extractionThe organic extract
  3. washwas washed with ice water and brine
  4. customdried
  5. filtrationfiltered
  6. customevaporated
  7. customto give a syrup, which
  8. customwas further dried at high vacuum
  9. temperaturecooled in dry ice/acetone

출처 및 근거

ORD 기록
ord-1b01b77d58b0472cbe68b93b4247487f
출처 데이터셋
uspto-grants-1986_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04593029

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