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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 61289Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium SulfateHCID 24436—
Edukt2,2-Difluoro-2-(fluorosulfonyl)acetic acidHCID 2737516—
EduktN-Boc-DL-serine Benzyl EsterHCID 12953535—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelAcetonitrileHCID 6342—
Produkt(S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl esterHCID 9004147340%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09441012B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-fdbbf23e8ab34ac6a6515ce0bc08c2cd
Quellennotizuspto-grants-2016_09