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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928055Generated: October 30, 2026

Benzyl Bromide → benzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate

https://huagongshe.com/reaction/928055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(3S)-1-[(tert-butoxy)carbonyl]pyrrolidine-3-carboxylic acidHCID 1512492—
SolventTolueneHCID 1140—
Productbenzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylateHCID 59016658—

Reaction Steps

DBU (0.764 mL) was added to a mixture of benzyl bromide (0.61 mL), (S)-1-tert-butoxycarbonyl-pyrrolidine-3-carboxylic acid (1 g) in anhydrous toluene (10 mL) and the mixture was stirred at room temperature for 24 hours. The mixture was filtered and the filtrate was concentrated in vacuo. The residue was purified by chromatography on silica eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-35% to give benzyl (S)-1-tert-butoxycarbonylpyrrolidine-3-carboxylate (0.859 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290472B2
Source datasetuspto-grants-2016_03
ORD IDord-68de794ff3c6415c8404db350a5cfa37
Source noteuspto-grants-2016_03