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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381887Generated: November 1, 2026

3-Bromopropylamine hydrobromide → Benzyl 3-bromopropylcarbamate

https://huagongshe.com/reaction/2381887

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromopropylamine hydrobromideHCID 78701—
ReactantBenzyl succinimido carbonateHCID 83172—
SolventDichloromethaneHCID 6344—
ProductBenzyl 3-bromopropylcarbamateHCID 25443692.1%

Reaction Steps

TEA (6.91 g, 68.5 mmol) was added drop wise to an ice-cooled mixture of 3-bromopropylamine.hydrobromide (10.0 g, 45.6 mmol) and N-(Benzyloxycarbonyloxy)-succinimide (11.22 g, 47.9 mmol) in DCM (200 mL). The stirred mixture was allowed to warm to Rt overnight, then washed with water, brine, dried (MgSO4), filtered and concentrated, providing 11.43 g (92%) of N-(Benzyloxycarbonyl)-3-bromopropylamine, as a pale yellow oil. 1H NMR (CDCl3): 7.35 (m, 5H), 5.10 (s, 2H), 4.89 (br s, 1H), 3.44 (t, J=6.6 Hz), 3.35 (dd, J=12.9, 6.3 Hz, 2H), m (2.06, 2H). LCMS (LC: Hydrophobic/TFA, RT=6.4 min; MS: 294, 296 ([M+NH4]+, 22%), 272, 274 ([M+H]+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258259B2
Source datasetuspto-grants-2012_09
ORD IDord-8fd2d9e6c9eb4496954ef66c40393d73
Source noteuspto-grants-2012_09