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Triethylamine → 3-(Benzo-1,2,3-thiadiazole-7-carbonyloxy)-5,5-dimethyl-cyclohex-2-enone

HRID 6360
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HRID 6360 반응식
[CH3:1][C:2]1([CH3:10])[CH2:7][C:6](=[O:8])[CH2:5][C:4](=[O:9])[CH2:3]1.C(N(CC)CC)C.[S:18]1[C:22]2[C:23]([C:27](Cl)=[O:28])=[CH:24][CH:25]=[CH:26][C:21]=2[N:20]=[N:19]1>C(OCC)(=O)C>[S:18]1[C:22]2[C:23]([C:27]([O:8][C:6]3[CH2:7][C:2]([CH3:10])([CH3:1])[CH2:3][C:4](=[O:9])[CH:5]=3)=[O:28])=[CH:24][CH:25]=[CH:26][C:21]=2[N:20]=[N:19]1
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 31358DimedoneHCID 183776071,2,3-Benzothiadiazole-7-carbonyl chloride

생성물 1

HCID 197934183-(Benzo-1,2,3-thiadiazole-7-carbonyloxy)-5,5-dimethyl-cyclohex-2-enone수율 87.5%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

5.6 g (0.04 mol) of 5,5-dimethyl-1,3-cyclohexanedione are dissolved in a mixture of 4.4 g (0.044 mol) of triethylamine and 120 ml of ethyl acetate. 8.7 g (0.044 mol) of benzothiadiazole-7-carboxylic acid chloride are added dropwise at 15° to 20° C., and the mixture is subsequently stirred overnight at room temperature. The ethyl acetate solution is washed with H2O, dried and concentrated. Purification by column chromatography using ethyl acetate/hexane gives 10.5 g (87.5%) of the title compound, melting point 131°-133° C.

후처리

  1. washThe ethyl acetate solution is washed with H2O
  2. customdried
  3. concentrationconcentrated
  4. customPurification by column chromatography

출처 및 근거

ORD 기록
ord-8e967b2fdeb8454a83c24e9d3bcde951
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05248683

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