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HRID 430482作成日:2026年10月24日

Butanal → 3-Methyl-3,5-heptanediol

https://huagongshe.com/ja/reaction/430482

反応式

関与物質

役割名称HCID仕込み量
反応物ButanalHCID 261—
反応物IsobutyraldehydeHCID 6561—
反応物2-Ethyl-1,3-HexanediolHCID 7211—
反応物2,2,4-Trimethyl-1,3-pentanediolHCID 8946—
反応物2,2-Dimethyl-1,3-hexanediolHCID 89569—
反応物3,5-OctanediolHCID 9812809—
反応物2-Ethyl-4-methyl-1,3-pentanediolHCID 10953660—
反応物2,2,3-Trimethyl-1,3-pentanediolHCID 21908643—
反応物2-Methyl-3,5-heptanediolHCID 22323945—
反応物2-Ethyl-3-methyl-1,3-pentanediolHCID 22323954—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物3-Methyl-3,5-heptanediolHCID 251263—

反応手順

The reaction of Condition A above is repeated, except that about one mole each of butyraldehyde, isobutyraldehyde, and 2-butanone are used. The condensation and reduction proceed analogously to yield a mixture of 8-carbon-1,3-diols primarily consisting of: 2,2,4-trimethyl-1,3-pentanediol; 2-ethyl-1,3-hexanediol; 2,2-dimethyl-1,3-hexanediol; 2-ethyl-4-methyl-1,3-pentanediol; 2-ethyl-3-methyl-1,3-pentanediol; 3,5-octanediol; 2,2,3-trimethyl-1,3-pentanediol; 2-methyl-3,5-heptanediol; and 3-methyl-3,5-heptanediol, along with other minor isomers resulting from condensation on the methylene of 2-butanone instead of the methyl.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06323172B1
出典データセットuspto-grants-2001_11
ORD IDord-151a6f1e570e4388ae0a7f4614e2d047
出典メモuspto-grants-2001_11