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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36182Generated: October 27, 2026

Benzyl chloroformate → Benzyl 3-bromopropylcarbamate

https://huagongshe.com/reaction/36182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
Reactant3-Bromopropylamine hydrobromideHCID 78701—
ReactantDiisopropylethylamineHCID 81531—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl 3-bromopropylcarbamateHCID 25443662.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of 3-bromopropylamine hydrobromide (2 g, 9.14 mM) in 40 mL dry THF was added, via hypodermic syringe, benzyl chloroformate (1.64 g, 9.60 mM) at room temperature. After cooling to 0° C., diisopropylethylamine (1.6 mL, 9.20 mM) was added dropwise via syringe and the reaction mixture was allowed to stir at 0° C. for 1 hour. The crude reaction mixture was filtered over a pad of Celite and solvents were evaporated. The residue was flash chromatographed on silica gel, eluting with 10-20-30% EtOAc/hexane to afford 1.56 g desired product as a liquid, homogeneous by TLC in 80:20 hexane-EtOAc;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411980
Source datasetuspto-grants-1995_05
ORD IDord-e1b2cbc13a4d4e269a66fa91b9949ec9
Source noteuspto-grants-1995_05