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HRID 328903作成日:2026年10月25日

3-Benzyloxy-1-(tert.butyl)azetidine → 1-tert-Butyl-3-hydroxyazetidine

https://huagongshe.com/reaction/328903

反応式

関与物質

役割名称HCID仕込み量
反応物3-Benzyloxy-1-(tert.butyl)azetidineHCID 20517332—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
生成物1-tert-Butyl-3-hydroxyazetidineHCID 28798676%

反応条件

温度40 °C

反応手順

A solution of 4.4 parts of 3-benzyloxy-1-(tert.butyl)azetidine in 30 parts of ethanol was taken into an autoclave together with 2 parts of Raney nickel as catalyst. Under a hydrogen gas pressure of 100 atmospheres, the mixture was stirred at 40° C. for 15 hours to perform the reduction. The catalyst was separated by filtration, and the remaining ethanol solution was concentrated to dryness. The resulting oily substance was dissolved in n-hexane and cooled. As a result 2.0 parts of 1-(tert.-butyl)-3-azetidinol melting at 42° - 43° C. The yield was 76%. The results of infra-red spectrum analysis and nuclear magnetic resonance analysis of the product are as follows:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04018824
出典データセットuspto-grants-1977_04
ORD IDord-db82225784564761821714242e8703a7
出典メモuspto-grants-1977_04