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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274918Generated: November 1, 2026

(+-)-3-Quinuclidinol → Quinuclidin-3-yl2-bromophenylcarbamate

https://huagongshe.com/reaction/2274918

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantSodium hydrideHCID 24758—
Reactant2-Bromophenyl isocyanateHCID 137097—
SolventTetrahydrofuranHCID 8028—
ProductQuinuclidin-3-yl2-bromophenylcarbamateHCID 6832776582%

Reaction Steps

To a solution of quinuclidin-3-ol (382 mg, 3.00 mmol) in THF (15 mL) was added NaH [60% dispersion in mineral oil] (156 mg, 3.90 mmol) at room temperature. The mixture was stirred for 15 min and 2-bromophenyl isocyanate (594 mg, 3.00 mmol) was added under stirring. The resulting mixture was stirred at room temperature for 18 h, quenched with brine and extracted with EtOAc. The organic layers were combined, dried over Na2SO4 and concentrated. The resulting crude product was purified by silica gel column chromatography (EtOAc/methanol 3:1) to give the product quinuclidin-3-yl 2-bromophenylcarbamate as viscous oil (0.80 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126993B2
Source datasetuspto-grants-2015_09
ORD IDord-0c32982d12da42279f7b5219d0c012fb
Source noteuspto-grants-2015_09