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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281257Generated: November 2, 2026

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

https://huagongshe.com/reaction/2281257

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 numberUS09139580B2
Source datasetuspto-grants-2015_09
ORD IDord-a04cc68ceed8444e8bff8a2f3ea6feee
Source noteuspto-grants-2015_09