Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698403Generated: October 30, 2026

1,4-Dibromobutane → 1-(4-Bromo-2-tert-butyl-phenyl)-pyrrolidine

https://huagongshe.com/reaction/1698403

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantSodium hydrideHCID 24758—
Reactant4-bromo-2-tert-butylphenylamineHCID 11959000—
Product1-(4-Bromo-2-tert-butyl-phenyl)-pyrrolidineHCID 6667226161.2%

Reaction Steps

In a manner analogous to example 1 b, the process is carried out by a reaction of 10 g (44 mmol) of 4-bromo-2-tert-butylphenylamine with 3.8 g (96 mmol) of 60% sodium hydride and with 3.4 ml (96 mmol) of 1,4-dibromobutane. 7.6 g of 1-(4-bromo-2-tert-butylphenyl)-pyrrolidine are obtained in the form of an oil (yield=61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163952B2
Source datasetuspto-grants-2012_04
ORD IDord-dab554a2275f4709aa55977e66c0f311
Source noteuspto-grants-2012_04