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HRID 1650961作成日:2026年10月27日

Hydrochloric Acid → 4-Amino-4-(1-(4-chlorophenyl)cyclobutyl]butan-1-ol

https://huagongshe.com/reaction/1650961

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3-Chloro-1-propanolHCID 12313—
反応物1-(4-Chlorophenyl)cyclobutanecarbonitrileHCID 98621—
反応物Sodium borohydrideHCID 4311764—
反応物MagnesiumHCID 5462224—
反応物HCID 178418918HCID 178418918—
溶媒WaterHCID 962—
溶媒IsopropanolHCID 3776—
溶媒TetrahydrofuranHCID 8028—
生成物4-Amino-4-(1-(4-chlorophenyl)cyclobutyl]butan-1-olHCID 19823713—

反応手順

A solution of 3-chloropropan-1-ol (95 ml) in tetrahydrofuran cooled to below -5° C. was added over 30 minutes to a solution of isopropylmagnesium chloride [prepared from magnesium (30 g), 2-chloropropane (100 ml) and tetrahydrofuran (300 ml)]. Magnesium (36 g) was added and the mixture warmed to initiate the reaction which then had to be cooled. Tetrahydrofuran (300 ml) was then added and the mixture heated under reflux for 30 minutes. 1-(4-Chlorophenyl)cyclobutanecarbonitrile (90 g) was added and the mixture heated under reflux for 16 hours and then cooled. Sodium borohydride (30 g) and then propan-2-ol (250 ml) were added and the mixture heated under reflux for 5 hours. The reaction mixture was poured into water (1 l), and acidified with excess concentrated hydrochloric acid. The resulting acidic mixture was extracted with toluene. Removal of the toluene gave a residue which was triturated with ether to give a solid which was dried, basified and extracted with ether. The ether was removed by evaportion to give a residue which was distilled (180°/1 mm to 172°/0.8 mm) to give 4-amino-4-(1-(4-chlorophenyl)cyclobutyl]butan-1-ol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04925879
出典データセットuspto-grants-1990_05
ORD IDord-3eadb3ab58f14c64be7f7c81d5786825
出典メモuspto-grants-1990_05