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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1527376Erstellt: 26. Oktober 2026

Benzyl Alcohol → N-(tert-Butoxycarbonyl)-(2S,4R)-4-fluoroproline benzyl ester

https://huagongshe.com/reaction/1527376

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzyl AlcoholHCID 244—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt(2S,4R)-1-[(tert-butoxy)carbonyl]-4-fluoropyrrolidine-2-carboxylic acidHCID 12043048—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(tert-Butoxycarbonyl)-(2S,4R)-4-fluoroproline benzyl esterHCID 68554319—

Reaktionsschritte

To a suspension of N-Boc-trans-4-fluoro-L-proline (4.5 g, 19.29 mmol) in CH2Cl2 (68 mL) were added DCC (4.78 g, 23.15 mmol), DMAP (0.236 g, 1.93 mmol) and benzyl alcohol (2 mL, 19.29 mmol). The resulting white suspension was stirred at RT for 48 h and filtered. The filtrate was concentrated to give a colorless oil which was purified by flash column chromatography on silica gel (c-hexane to c-hexane/EtOAc 4-1) to give the desired compound. TLC, Rf (c-hexane/EtOAc 3:1)=0.3; MS: 346.0 [M+Na]+; tR (HPLC conditions a): 3.85 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09085555B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-890d4d9ea2e646c681ccb6cd502039f6
Quellennotizuspto-grants-2015_07