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Oxygen → 2,5-Dimethyl-4-hydroxy-tetrahydrofuran-3-one

HRID 1578017
ノート
印刷プレビュー

反応式

HRID 1578017 の反応式
[CH3:1][CH:2]1[CH:6]([OH:7])[CH:5]([OH:8])[CH:4]([CH3:9])[O:3]1.O=O>[Ag].[Cu]>[CH3:1][CH:2]1[C:6](=[O:7])[CH:5]([OH:8])[CH:4]([CH3:9])[O:3]1
参加物実験手順出典と根拠反応ノート

参加物

5

反応物 2

HCID 977OxygenHCID 204869562,5-Dimethyl-3,4-dihydroxy-tetrahydrofuran

生成物 1

HCID 103131462,5-Dimethyl-4-hydroxy-tetrahydrofuran-3-one

試薬・触媒・溶媒 2

HCID 23954Silver触媒HCID 23978Copper触媒

実験手順

2,5-Dimethyl-4-hydroxy-2,3-dihydrofuran-3-one is prepared by first epoxidizing hex-3-ene-2,5-diol in the liquid phase with hydrogen peroxide to give the novel compound 3,4-epoxy-hexane-2,5-diol, which at 40°-280° C. is converted, by means of a catalytic amount of an acid, to the novel compound 2,5-dimethyl-3,4-dihydroxy-tetrahydro-furan. The latter is dehydrogenated by means of oxygen over a silver catalyst or copper catalyst to give the nove compound 2,5-dimethyl-4-hydroxy-tetrahydrofuran-3-one, which is oxidized by means of bismuth oxide, in concentrated acetic acid solution, to give the desired compound 2,5-dimethyl-4-hydroxy-2,3-dihydrofuran-3-one.

出典と根拠

ORDレコード
ord-b09a9443421c457c95337c00953f202f
出典データセット
uspto-grants-1981_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04290960

反応ノート

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