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5,6-Dimethyl-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione → HCID 54268221, 화합물

HRID 745204
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HRID 745204 반응식
[CH3:1][C:2]1[CH2:3][CH:4]2[C:12](=[O:13])[O:11][C:9](=[O:10])[CH:5]2[CH2:6][C:7]=1[CH3:8]>[Pt](=O)=O.O1CCCC1>[CH3:1][CH:2]1[CH:7]([CH3:8])[CH2:6][C:5]2[C:9]([O:11][C:12](=[O:13])[C:4]=2[CH2:3]1)=[O:10]
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참가 물질

4

반응물 1

HCID 2262975,6-Dimethyl-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione

생성물 1

HCID 54268221HCID 54268221, 화합물

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 8028Tetrahydrofuran용매

실험 절차

A mixture of 4,5-dimethyl-4-cyclohexene-1,2-dicarboxylic anhydride (10 g; 0.0555 mol), platinum dioxide (150 mg) and tetrahydrofuran (100 ml) was hydrogenated at room temperature for 8 hours. Precipitates were removed by filtration, and the filtrate was evaporated under reduced pressure to give 4,5-dimethylcyclohexene-1,2-dicarboxylic anhydride. IR νmaxFilm (cm-1): 1860, 1760.

후처리

  1. customPrecipitates
  2. customwere removed by filtration
  3. customthe filtrate was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-3d71c9372df04af1a1a56555ab099c4b
출처 데이터셋
uspto-grants-1986_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04598078

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