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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 61289생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/61289

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfateHCID 24436—
반응물2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
반응물N-Boc-DL-serine Benzyl EsterHCID 12953535—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Diethyl EtherHCID 3283—
용매AcetonitrileHCID 6342—
생성물(S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl esterHCID 9004147340%

반응 조건

온도60 °C

반응 단계

To a stirred solution of the compound of Formula XII(a), benzyl 2-(tert-butoxycarbonylamino)-3-hydroxypropanoate (1 g, 3.38 mmol) in acetonitrile (10 mL) was added copper(I) iodide (64.4 mg, 0.338 mmol) and sodium sulfate (48.1 mg, 0.338 mmol). The resulting mixture was stirred at 60° C. and treated with 2,2-difluoro-2-fluorosulfonylacetic acid (524 μL, 5.08 mmol), dropwise, as a solution in acetonitrile (2 mL) over a period of 1.5 h. Upon completion of the addition, the mixture was stirred for a further 30 min then cooled to room temperature. The mixture was diluted with diethyl ether and washed with brine (2×), water (3×) and brine (1×). The organic phase was dried, filtered and concentrated in vacuo then chromatographed in 0-30% ethyl acetate in hexanes, to provide the compound of Formula XIII(a), (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester (458 mg, 40%) as a colorless sticky oil. 1H NMR (300 MHz, CDCl3): δ (ppm) 7.32-7.38 (m, 5H), 6.18 (wt, 1H), 5.28 (dd, 1H), 5.19 (dd, 2H), 4.55 (dt, 1H) 4.22 (td, 1H), 4.15 (m, 2H), 1.38 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09441012B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-fdbbf23e8ab34ac6a6515ce0bc08c2cd
출처 메모uspto-grants-2016_09