反応式
[CH2:1](O)[CH2:2][CH2:3][CH2:4]O.[C:7]([O:10][CH:11]=[CH:12][CH2:13][CH2:14][O:15][C:16](=[O:18])[CH3:17])(=[O:9])[CH3:8]>O1CCCC1>[CH2:1]=[CH:2][CH:3]=[CH2:4].[C:7]([O:10][CH2:11][CH2:12][CH2:13][CH2:14][O:15][C:16](=[O:18])[CH3:17])(=[O:9])[CH3:8]参加物
5
実験手順
The process for preparing tetrahydrofuran according to claim 1, wherein 1,4-butanediol is prepared by hydrogenating 1,4-diacetoxybutene, which is produced by the acetoxylation of butadiene, into 1,4-diacetoxybutane and hydrolyzing said 1,4-diacetoxybutane as the hydrogenated products in the presence of a solid acid catalyst and distilling hydrolyzates thus obtained.
出典と根拠
- ORDレコード
- ord-357e585483c74cd09deece7735851e7f
- 出典データセット
- uspto-grants-1978_06
- 特許番号
- US04093633
関連ノート
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