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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260282Generated: November 1, 2026

Carbon tetrabromide → 3-Bromo-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1260282

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Boc-3-pyrrolidinolHCID 4416939—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 42614217—

Reaction Steps

Triphenylphosphine (727 mg, 2.77 mmol) was added to a stirred solution of tert-butyl 3-hydroxypyrrolidine-1-carboxylate (173 mg, 0.924 mmol) and carbon tetrabromide (919 mg, 2.77 mmol) in THF (3.00 mL) at 0° C., and the resulting mixture was allowed to warm slowly to rt. After 20 h, the reaction was filtered and concentrated in vacuo. Purification of the crude residue by flash chromatography on silica gel (gradient elution; 10%-40% EtOAc/hexanes as eluent) afforded the title compound i-4-a. m/z (ES) 250 (MH)+. 1H NMR (500 MHz, CDCl3): δ 4.49 (m, 1H), 3.81 (m, 2H), 3.63 (m, 1H), 3.53 (m, 1H), 2.33 (m, 1H), 2.26 (m, 1H), 1.49 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470819B2
Source datasetuspto-grants-2013_06
ORD IDord-b2b768af207741298559bc4149d2a53c
Source noteuspto-grants-2013_06