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Methanesulfonyl chloride → Methanesulfonic acid 1-methyl-2-(1-phenyl-2,5-cyclohexadien-1-yl)-ethyl ester

HRID 2287125
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HRID 2287125 반응식
[CH3:1][CH:2]([OH:16])[CH2:3][C:4]1([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:9]=[CH:8][CH2:7][CH:6]=[CH:5]1.[S:17](Cl)([CH3:20])(=[O:19])=[O:18]>N1C=CC=CC=1>[CH3:1][CH:2]([O:16][S:17]([CH3:20])(=[O:19])=[O:18])[CH2:3][C:4]1([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][CH2:7][CH:8]=[CH:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31297Methanesulfonyl chlorideHCID 23459447alpha-Methyl-1-phenyl-2,5-cyclohexadien-1-ethanol

생성물 1

HCID 53747931Methanesulfonic acid 1-methyl-2-(1-phenyl-2,5-cyclohexadien-1-yl)-ethyl ester

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

8 g. of α-methyl-1-phenyl-2,5-cyclohexadien-1-ethanol are dissolved in 50 ml. of pyridine and 6.4 g. of mesyl chloride are added dropwise at 0°-5° C. After stirring at room temperature for 2 hours, the mixture is worked-up as follows: The mixture is treated with ice-water and extracted with ether. The ether phase is washed with 3 N aqueous hydrochloric acid, then washed neutral, dried and concentrated. The crude product obtained is chromatographed on 100 g. of silica gel with ether/petroleum ether (1:1). There is obtained an oily product which crystallizes in the cold. After crystallization from methylene chloride/hexane, there is obtained methanesulfonic acid 1-methyl-2-(1-phenyl-2,5-cyclohexadien-1-yl)-ethyl ester having a melting point of 51°-53° C.

후처리

  1. extractionextracted with ether
  2. washThe ether phase is washed with 3 N aqueous hydrochloric acid
  3. washwashed neutral
  4. customdried
  5. concentrationconcentrated
  6. customThe crude product obtained
  7. customis chromatographed on 100 g
  8. customThere is obtained an oily product which
  9. customcrystallizes in the cold
  10. customAfter crystallization from methylene chloride/hexane

출처 및 근거

ORD 기록
ord-f7b1015871e149a2997297cc98245691
출처 데이터셋
uspto-grants-1981_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04269788

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