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HRID 70106作成日:2026年10月24日

Methyl iodide → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid

https://huagongshe.com/ja/reaction/70106

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物N-[tert-butoxycarbonyl]-L-serineHCID 98766—
反応物Sodium ethoxideHCID 2723922—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物(2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acidHCID 7016354—

反応手順

Under nitrogen a mixture of 74 ml abs. THF and 6 ml abs. methanol is cooled to −70° C. and 2 g sodium hydride (55-65% dispersion) are added. The suspension is stirred for 0.4 hour at ambient temperature. Under nitrogen, 2.05 g N-Boc-L-serine are suspended in 100 ml abs. THF and 40 ml of the prepared sodium ethoxide solution are added. The suspension is stirred for 1 hour at ambient temperature and 1 ml methyliodide are added. After 1 hour the remainder of the sodium ethoxide solution and another 2 ml of methyliodide are added. After 18 hours the reaction mixture is evaporated to dryness. The residue is washed with water and ether and extracted. The water phase is acidified and extracted with ethyl acetate and dichloromethane. 0.52 g of the product are obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822474B2
出典データセットuspto-grants-2014_09
ORD IDord-1a7854345f3e4da0922298bdc2c9bd38
出典メモuspto-grants-2014_09