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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243084Generated: October 30, 2026

Benzyl Bromide → HCID 178454132, compound

https://huagongshe.com/reaction/243084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178454126HCID 178454126—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178454132HCID 17845413272%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl(trans-3-hydroxycyclobutyl)carbamate (0.93 g, 4.97 mmol) was dissolved in dry THF (20 mL) under a nitrogen atmosphere, and the solution cooled to 0° C. To this clear solution, sodium hydride (60% dispersion in oil, 0.2 g, 4.97 mmol) was added portion wise (evolution of H2 observed). The mixture was stirred at RT for 30 min then benzyl bromide (0.88 mL, 7.45 mmol) added dropwise and the resulting dark brown suspension stirred at rt for 16 h. The reaction mixture was quenched with saturated aqueous NH4Cl (20 mL) and partitioned between saturated aqueous 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 off-white solid (0.99 g, 72%). 1H NMR (CDCl3, 400 MHz): δ 7.35-7.31 (5H, m), 4.65 (1H, br, NH), 4.40 (2H, s), 4.24-4.12 (2H, m), 2.50-2.35 (2H, m), 2.18-2.06 (2H, m), 1.43 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653089B2
Source datasetuspto-grants-2014_02
ORD IDord-dcc60984a712491a88c49ab78df92a25
Source noteuspto-grants-2014_02