2,5-Dimethylphenol → 2,5-Dimethylhydroquinone

HRID 1678942

反応式

HRID 1678942 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[OH:9].CC1C=C([OH:18])C=C(C)C=1.CC1C=CC(C)=C(O)C=1O>>[CH3:1][C:2]1[CH:7]=[C:6]([OH:18])[C:5]([CH3:8])=[CH:4][C:3]=1[OH:9]

参加物

4

反応物 3

HCID 72672,5-DimethylphenolHCID 79483,5-DimethylphenolHCID 114691143,6-Dimethylbenzene-1,2-diol

生成物 1

HCID 692112,5-Dimethylhydroquinone

実験手順

By following in the same manner as in Example 53, except that 100 g. (819 m. moles) of 2,5-dimethylphenol were used instead of 3,5-dimethylphenol, 1.45 g. (10.5 m. moles) of 3,6-dimethylcatechol and 1.85 g. (13.4 m. moles) of 2,5-dimethylhydroquinone were obtained. The yield of dihydric alkylphenols was 46.9 percent.

出典と根拠

ORDレコード
ord-e2347731fae14699b065d71fe5c2939b
出典データセット
uspto-grants-1978_03
特許番号
US04078006

関連ノート

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