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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 321948Generated: October 29, 2026

Benzyl Bromide → N-Boc-N-benzyl-3-chloropropylamine

https://huagongshe.com/reaction/321948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantN-Boc-3-ChloropropylamineHCID 10932310—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductN-Boc-N-benzyl-3-chloropropylamineHCID 1109806213.4%

Reaction Steps

To a solution of N-Boc-3-chloropropylamine (10.0 g, 51.8 mmol) in THF was added sodium hydride (1.87 g, 78 mmol). After 20 min, benzyl bromide (9.24 mL, 78 mmol) was added and the reaction mixture was heated at reflux for 16 h. After cooling, the reaction mixture was diluted with Et2O (150 mL) and H2O (50 mL), the layers were separated and the aqueous layer was extracted twice with Et2O. The combined organic phases were washed with H2O and brine, dried (MgSO4), filtered and concentrated. The resulting yellow oil was purified by flash chromatography (SiO2, 10% EtOAc-hexane) to give N-Boc-N-benzyl-3-chloropropylamine (1.97 g, 13% yield) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211170B1
Source datasetuspto-grants-2001_04
ORD IDord-256e366c627e4932a36fa4f2e340f0d0
Source noteuspto-grants-2001_04