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HRID 534679作成日:2026年10月26日

Dichloromethane → N-benzyl-O-benzyl-D-serinamide

https://huagongshe.com/reaction/534679

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Trifluoroacetic acidHCID 6422—
反応物Sodium HydroxideHCID 14798—
反応物N-benzyl-O-benzyl-N2-Boc-D-serinamideHCID 7216909—
溶媒WaterHCID 962—
生成物N-benzyl-O-benzyl-D-serinamideHCID 6708283390.1%

反応手順

To a solution of N-benzyl-O-benzyl-N2-Boc-D-serinamide (30 g) and dichloromethane (150 mL), trifluoroacetic acid (150 mL) was added. The solution was stirred for 2 hours at room temperature for completion of reaction. The solution was concentrated under vacuum to obtain solid which was dissolved in water. The aqueous layer was basified to pH 8-10 with 5% sodium hydroxide. The aqueous layer was extracted with ethyl acetate and the combined organic layers washed with brine solution. Organic layer was concentrated under vacuum to obtain an oily residue solidify by n-Hexane to give 20 g of N-benzyl-O-benzyl-D-serinamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853439B2
出典データセットuspto-grants-2014_10
ORD IDord-be2f9f7a3be14f24980bc1a11043ee1e
出典メモuspto-grants-2014_10