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HRID 236467作成日:2026年10月27日

L-Alanine → Boc-Gly-Ala-OH

https://huagongshe.com/reaction/236467

反応式

関与物質

役割名称HCID仕込み量
反応物L-AlanineHCID 5950—
反応物TriethylamineHCID 8471—
反応物N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
反応物N-HydroxysuccinimideHCID 80170—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物Boc-Gly-Ala-OHHCID 1112859041.5%

反応手順

Boc-Gly-Ala-OH was prepared by an N-hydroxysuccinimide coupling procedure. Boc-Gly-OSu (7.67 g, 28.2 mmol) was dissolved in 10 mL of dimethylsulfoxide and the resulting solution was added to a solution consisting of H-Ala-OH (3.76 g, 42.3 mmol) and triethylamine (5.89 mL, 42.3 mmol) in 20 mL of water. After stirring overnight, a precipitate was removed by filtration. The remaining solution was diluted with water and then acidified with hydrochloric acid. An aqueous phase separated from which product was extracted by addition of ethyl acetate. The ethyl acetate extract was washed with 0.2N hydrochloric acid and then saturated sodium chloride prepared in 0.2N hydrochloric acid. The washed ethyl acetate solution was then dried over sodium sulfate and filtered. Solvent was then evaporated, leaving a foamy product, which was crystallized from ethyl acetate:hexane to yield 2.88 g of Boc-Gly-Ala-OH (m.p. 128°-130°).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04644055
出典データセットuspto-grants-1987_02
ORD IDord-5f4e8b8470144a09bcc9d74752d34e24
出典メモuspto-grants-1987_02