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HRID 1940375作成日:2026年10月26日

Hydrochloric Acid → Triapenthenol

https://huagongshe.com/reaction/1940375

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物(S)-(-)-2-Amino-3-methyl-1,1-diphenyl-1-butanolHCID 854145—
反応物Borane;tetrahydrofuranHCID 2723981—
反応物(E)-1-cyclohexyl-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-oneHCID 12763477—
溶媒1,2-DichloroethaneHCID 11—
生成物TriapenthenolHCID 6437842—

反応手順

In a nitrogen atmosphere, a solution of 0.230 g (0.90 mmole) of (S)-2-amino-1,1-diphenyl-3-methylbutan-1-ol in 2.5 ml of 1,2-dichloroethane was added dropwise at -78° C. to a solution comprising 1.29 ml (0.90 mmole) of 0.70M borane-tetrahydrofuran solution and 1 ml of 1,2-dichloroethane, and the temperature of the mixture was raised from -78° C. to room temperature over about 2 hours. Thereafter, a solution of 0.157 g (0.6 mmole, E/Z=99.9/0.1) of (E)-1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-one in 2.5 ml of 1,2-dichloroethane was added dropwise to this solution, and stirring was carried out for 24 hours. The reaction product was decomposed with addition of 6 ml of 10% hydrochloric acid to the solution, and after removing (S)-2-amino-1,1-diphenyl-3-methylbutan-1-ol hydrochloride by filtration, the organic layer was washed with water and concentrated under reduced pressure to obtain crude (-)-(E)-1-cyclohexyl-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-1-penten-3-ol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05698742
出典データセットuspto-grants-1997_12
ORD IDord-349ae12b1eca47888d9b821b44834162
出典メモuspto-grants-1997_12