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HRID 61294생성일: 2026년 10월 26일

Proton sponge → (S)-2-tert-Butoxycarbonylamino-3-methoxypropionic acid benzyl ester

https://huagongshe.com/reaction/61294

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참여 물질

역할이름HCID투입량
반응물Proton spongeHCID 88675—
반응물Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 2735153—
반응물Boc-Ser-OBzlHCID 7018792—
용매DichloromethaneHCID 6344—
생성물(S)-2-tert-Butoxycarbonylamino-3-methoxypropionic acid benzyl esterHCID 1528780869.6%

반응 단계

To a solution of the compound of Formula XII(a), (S)-2-tert-butoxycarbonylamino-3-hydroxy-propionic acid benzyl ester (1.7 g, 5.76 mmol) in dichloromethane (50 mL) was added trimethyloxonium tetrafluoroborate (1.11 g, 7.50 mmol), followed by the portion-wise addition of proton sponge (1.61 g, 7.50 mmol). After stirring for 24 hrs at RT, the solution was concentrated, and the residue was dissolved in ethyl acetate, and the solution filtered through a pad of celite. The filtrate was washed with 1 M HCl and brine. The organic layers were dried over MgSO4, filtered, and concentrated in vacuo. Silica-gel flash chromatography with 5% to 15% ethyl acetate in hexanes afforded the compound of Formula XIII(b), (S)-2-tert-butoxycarbonylamino-3-methoxy-propionic acid benzyl ester (1.24 g, 69.6%) as a colorless oil. 1H NMR (300 MHz, CDCl3): δ (ppm) 7.35-7.29 (m, 5H), 4.90-4.87 (m, 1H), 4.51 (s, 2H), 3.92-3.87 (m, 1H), 3.80-3.78 (m, 1H), 3.56 (dd, 2H), 3.42 (dd, 1H), 3.33 (s, 3H), 1.42 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09441012B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-9782e5cd3b1345a4baac6656ba3a5fd9
출처 메모uspto-grants-2016_09