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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727545Generated: October 31, 2026

Benzyl Bromide → HCID 19705562, compound

https://huagongshe.com/reaction/727545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19705548HCID 19705548—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19705562HCID 19705562117.3%

Reaction Steps

A cold (0° C.) solution of tert-butyl 3-(2-methylpropyl)-2-oxo-α-(propen-2-yl)-3-pyrrolidineacetate (1.11 g, 3.76 mmol) in dry THF (25 mL) is treated with NaH (60% dispersion in mineral oil, 226 mg, 5.64 mmol) in one portion. After 30 minutes, benzyl bromide (537 μL, 4.51 mmol) is added. The solution is allowed to slowly warm to room temperature, stirring under N2 overnight. The mixture is quenched with H2O (25 mL) and extracted with EtOAc (3×25 mL). The organic extracts are combined, washed with brine (25 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to yield 1.70 g of yellow oil. The oil is purified by silica gel chromatography (30 g SG, 10% EtOAc/hexane) to give 1.37 g (94%) of the title compound as a clear, colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712300
Source datasetuspto-grants-1998_01
ORD IDord-fb08a005b27b4eefa167f0a4e2443dc9
Source noteuspto-grants-1998_01