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HRID 1752309作成日:2026年10月27日

Hydrochloric Acid → (S)-3-hydroxy-pyrrolidine-1-carboxylic acid 5-hydroxy-adamantan-2-yl ester

https://huagongshe.com/reaction/1752309

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TriphosgeneHCID 94429—
反応物(3S)-pyrrolidin-3-olHCID 2733874—
反応物Adamantane-1,4-diolHCID 4252005—
溶媒PyridineHCID 1049—
溶媒DichloromethaneHCID 6344—
生成物(S)-3-hydroxy-pyrrolidine-1-carboxylic acid 5-hydroxy-adamantan-2-yl esterHCID 58171511—

反応条件

温度-10 °C

反応手順

Triphosgene (0.58 g) dissolved in dichloromethane (10 mL) is added dropwise to a solution of adamantane-1,4-diol (1.00 g) and pyridine (10 mL) in dichloromethane (30 mL) cooled to −10° C. The solution is stirred at ca. 0° C. for 2.5 h and then (S)-3-hydroxy-pyrrolidine (0.50 mL) is added. The resulting solution is stirred overnight while warming to room temperature. The solution is then diluted with dichloromethane (50 mL) and chilled in an ice bath. 4 M hydrochloric acid (25 mL) is added and the resulting mixture is stirred for 5 min. The organic phase is separated and washed with 4 M hydrochloric acid and water. The organic phase is dried (MgSO4) and concentrated to give the title compound as a mixture of diastereomers (ca. 1:1). Yield: 0.98 g (59% of theory); Mass spectrum (ESI+): m/z=282 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09163012B2
出典データセットuspto-grants-2015_10
ORD IDord-aa4f94b162ee4f46bfbaeb81dc283bc1
出典メモuspto-grants-2015_10