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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243078Generated: October 31, 2026

Benzyl Bromide → HCID 178454131, compound

https://huagongshe.com/reaction/243078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178454125HCID 178454125—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178454131HCID 17845413181%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl(cis-3-hydroxycyclobutyl)carbamate (2.0 g, 10.7 mmol) was dissolved in dry THF (50 mL) under nitrogen atmosphere, and the solution cooled to 0° C. To this clear solution, sodium hydride (60% dispersion in oil, 0.428 g, 10.7 mmol) was added portion wise (evolution of H2 observed). The mixture was stirred at rt for 30 min then benzyl bromide (1.91 mL, 16.04 mmol) added dropwise and the resulting yellow suspension stirred at rt for 16 h. The reaction was quenched with sat aq. NH4Cl solution (20 mL) and partitioned between sat aq. NaHCO3 (40 mL) and DCM (60 mL). The combined organic fractions were washed with brine (20 mL), dried (MgSO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (gradient 0-50% EtOAc in cyclohexane) to afford the title compound as a white solid (2.40 g, 81%). 1H NMR (CDCl3, 400 MHz): δ 7.41-7.22 (5H, m), 4.66 (1H, br, NH), 4.42 (2H, s), 3.83-3.65 (2H, m), 2.79-2.61 (2H, m), 1.86-1.72 (2H, m), 1.46 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-298b9c2d30c04ba8a79712db228743a3
Source noteuspto-grants-2014_02