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Propargyl bromide → 5-Methyl-2-propargyloxyphenylsulfonamide

HRID 1248371
노트
인쇄 미리보기

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HRID 1248371 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[S:9]([NH2:12])(=[O:11])=[O:10].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Br)[C:20]#[CH:21]>C(#N)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([O:1][CH2:21][C:20]#[CH:19])=[C:3]([S:9]([NH2:12])(=[O:10])=[O:11])[CH:4]=1
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참가 물질

5

반응물 3

HCID 7842Propargyl bromideHCID 11430Potassium CarbonateHCID 133217532-Hydroxy-5-methylbenzenesulfonamide

생성물 1

HCID 134729485-Methyl-2-propargyloxyphenylsulfonamide

시약·촉매·용매 1

HCID 6342Acetonitrile용매

반응 조건

온도
50 °C

실험 절차

A mixture of 24.3 g of 2-hydroxy-5-methylphenylsulfonamide, 36.0 g of potassium carbonate, 16.7 g of propargyl bromide and 500 ml of acetonitrile is stirred at 50° C. for 4.5 hours. The reaction mixture is then filtered, and concentrated by evaporation. The yield after recrystallisation from ethyl acetate is 23.9 g of 5-methyl-2-propargyloxyphenylsulfonamide, m.p. 169°-170° C.

후처리

  1. filtrationThe reaction mixture is then filtered
  2. concentrationconcentrated by evaporation
  3. customThe yield
  4. customafter recrystallisation from ethyl acetate

출처 및 근거

ORD 기록
ord-127d623726274a86a75da5c167078b81
출처 데이터셋
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04523944

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