戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1530766作成日:2026年10月25日

Sodium Carbonate → (R)-methyl 1-(methoxyamino)-1-oxo-3-phenylpropan-2-ylcarbamate

https://huagongshe.com/reaction/1530766

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物O-Methylhydroxylamine hydrochlorideHCID 521874—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物(R)-2-(methoxycarbonylamino)-3-phenylpropanoic acidHCID 10799103—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物(R)-methyl 1-(methoxyamino)-1-oxo-3-phenylpropan-2-ylcarbamateHCID 10682227—

反応手順

A mixture of sodium carbonate (10.20 g, 96.2 mmol) in water (170 ml) is added to a mixture of (R)-2-(methoxycarbonylamino)-3-phenylpropanoic acid (II, EXAMPLE 1, ˜0.148 mol crude) in methylene chloride. Methoxylamine hydrochloride (14.2 g, 0.170 mol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) (31.21 g, 0.163 mol) are added, and the mixture is stirred at 20-25° for 22 hours. The mixture is diluted with tetrahydrofuran (to dissolve the precipitate) and the layers are separated. The aqueous layer is extracted with 1:1 tetrahydrofuran/ether, and the combined organic extracts are washed with hydrochloric acid (10%) and saturated sodium bicarbonate solution. The mixture is dried over magnesium sulfate, filtered and the solvent removed under reduced pressure. Crystallization from ethyl acetate gives the title compound, mp=154-155°; NMR (CDCl3) 3.05, 3.58, 3.61, 4.34, 5.66, 7.15-7.31 and 9.44 δ; IR (mineral oil) 1694 and 1668 cm−1; [a]25D=+5.2° (CH3OH, c=1.045).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06197339B1
出典データセットuspto-grants-2001_03
ORD IDord-2c6e66cc773b45f2b8381506c676008a
出典メモuspto-grants-2001_03