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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630072Generated: November 1, 2026

(2S,4R)-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate → (2S,4R)-N-(4-(4-fluorophenoxy)phenyl)-4-hydroxypyrrolidine-2-carboxamide

https://huagongshe.com/reaction/1630072

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 67010572—
SolventHydrochloric AcidHCID 313—
Product(2S,4R)-N-(4-(4-fluorophenoxy)phenyl)-4-hydroxypyrrolidine-2-carboxamideHCID 5695416251%

Reaction Steps

Step (b) (2S,4R)-tert-butyl 2-(4-(4-fluorophenoxy)phenylcarbamoyl)-4-hydroxypyrrolidine-1-carboxylate was combined with hydrogen chloride (4N in dioxane, 20 mL) and the mixture was stirred at ambient temperature for 1 hour and then quenched with saturated sodium bicarbonate (aq., 100 mL). This mixture was extracted with ethyl acetate (30 mL) and the extract was washed with deionized water (30 mL) and then brine (30 mL), dried over anhydrous sodium sulfate, filtered and concentrated. The residue was triturated with ethyl acetate to give (2S,4R)—N-(4-(4-fluorophenoxy)phenyl)-4-hydroxypyrrolidine-2-carboxamide (1.47 g, 4.65 mmol, 51% yield) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791102B2
Source datasetuspto-grants-2014_07
ORD IDord-ede87283d392426fa8321e0e045138dd
Source noteuspto-grants-2014_07