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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173081Generated: November 2, 2026

(2S,4S)-1-tert-Butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylate → (2S,4S)-4-Benzyloxycarbonylaminopyrrolidine-2-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/1173081

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4S)-1-tert-Butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylateHCID 57648857—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
Product(2S,4S)-4-Benzyloxycarbonylaminopyrrolidine-2-carboxylic Acid Methyl EsterHCID 4507252867.9%

Reaction Steps

(2S,4S)-4-Benzyloxycarbonylaminopyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-methyl ester (10.4 g, 28 mmol) was dissolved in a 4M solution of HCl in 1,4-dioxane. The solution was stirred at room temperature for 3 hours and then evaporated. The residue was partitioned between EtOAc (200 mL) and 1M NaOH (100 mL), the layers separated and the aqueous layer re-extracted with EtOAc (100 mL). The combined organics were washed with saturated aqueous NaCl (100 mL), dried over Na2SO4, and evaporated to afford the title compound (5.4 g, 19 mmol) as a white solid, which was used without further purification. MS m/z: [M+H]+ calcd for C14H18N2O4, 278.3. found 279.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834041B2
Source datasetuspto-grants-2010_11
ORD IDord-0557ddd714bb4508a126210d335c98a4
Source noteuspto-grants-2010_11