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HRID 61290作成日:2026年10月26日

(S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester → (S)-2-tert-Butoxycarbonylamino-3-difluoromethoxy-propionic acid

https://huagongshe.com/reaction/61290

反応式

関与物質

役割名称HCID仕込み量
反応物(S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl esterHCID 90041473—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-2-tert-Butoxycarbonylamino-3-difluoromethoxy-propionic acidHCID 86709693100.1%

反応手順

A solution of the compound of Formula XIII(a), (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester (1.76 g, 5.09 mmol) in THF was stirred with 10% Pd/C (360 mg) under a hydrogen atmosphere for 2 hours. The reaction mixture was filtered and concentrated to give the compound of Formula IV(a), (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid (1.3 g, 100%) as a sticky, colorless oil. 1H NMR (300 MHz, CDCl3): δ (ppm) 6.21 (wt, 1H), 5.35 (d, 1H), 4.59 (m, 1H), 4.35 (m, 1H), 4.21 (m, 1H) and 1.42 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09441012B2
出典データセットuspto-grants-2016_09
ORD IDord-7594e7f9c27343a4a2c736838633cf8d
出典メモuspto-grants-2016_09