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HRID 233339作成日:2026年10月24日

Hydrochloric Acid → methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate

https://huagongshe.com/ja/reaction/233339

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BromochloromethaneHCID 6333—
反応物ChlorotrimethylsilaneHCID 6397—
反応物(S)-Methyl 2-((methoxycarbonyl)amino)-3-phenylpropanoateHCID 10609905—
反応物HCID 178506865HCID 178506865—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamateHCID 988153370%

反応手順

15.4 ml of a 2.6 molar solution of hexyllithium in hexane were added dropwise at -80° C. to a solution of 9.50 g of methyl (S)-2-methoxycarbonylamino-3-phenyl-propionate in 60 ml of tetrahydrofuran. Subsequently, the mixture was treated with 5.60 ml of chlorotrimethylsilane. The resulting suspension was stirred and treated with 3.22 ml of bromochloromethane. Subsequently, 18.4 ml of hexyllithium solution were added. The solution was treated at -80° C. with 11 ml of 20% methanolic hydrochloric acid, warmed to 22° and diluted with 100 ml of water and 40 ml of tetrahydrofuran. The phases were separated and the organic phase was washed with saturated sodium chloride solution, dried and concentrated. The residue was recrystallized from ethyl acetate and hexane and the crystallizate was dried, there being obtained 7.20 g (70%) of pure methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate, m.p. 122°-123° C. IR (KBr): 3336s (NH), 1737s and 1686s (C=O), 1535s (amide II).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05591885
出典データセットuspto-grants-1997_01
ORD IDord-9bef9ffaabdf42c7983198d7d20b557d
出典メモuspto-grants-1997_01