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3-Bromotropolone → HCID 439776, 화합물

HRID 2052380
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인쇄 미리보기

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HRID 2052380 반응식
Br[C:2]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4](=[O:9])[C:3]=1[OH:10].[CH3:11][O-:12].[Na+].[Na]>CO>[OH:10][C:3]1[C:4](=[O:9])[CH:5]=[CH:6][CH:7]=[CH:8][C:2]=1[O:12][CH3:11]
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참가 물질

5

반응물 3

HCID 207183-BromotropoloneHCID 5360545SodiumHCID 10942334Sodium Methoxide

생성물 1

HCID 439776HCID 439776, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

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온도
80 °C

실험 절차

A solution of 3-bromo-2-hydroxy-2,4,6-cycloheptatrien-1-one [27.5 g, described by T. Toda et al., Nippon Kagaku Zasshi, 88, 1234-5 (1967), (CA 68 101342)] and sodium methoxide (prepared from 12.6 g of sodium in methanol followed by evaporation of the methanol) in dimethyl sulfoxide (300 ml) is heated at 80° C. for one hour. The solution is cooled poured on ice, acidified with 2N sulfuric acid and extracted with ethyl acetate. The organic extract is washed with brine, dried over sodium sulfate and evaporated. The residue is crystallized from ethyl acetate-hexane to give 2-hydroxy-3-methoxy-2,4,6-cycloheptatrien-1-one. Evaporation of the mother liquors gives 2-hydroxy-4-methoxy-2,4,6-cycloheptatrien-1-one.

후처리

  1. customfollowed by evaporation of the methanol) in dimethyl sulfoxide (300 ml)
  2. temperatureThe solution is cooled
  3. additionpoured on ice
  4. extractionextracted with ethyl acetate
  5. extractionThe organic extract
  6. washis washed with brine
  7. dry with materialdried over sodium sulfate
  8. customevaporated
  9. customThe residue is crystallized from ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-1e0a74d6ca0140f8ba552f5566d65d7d
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04183955

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