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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567844Generated: October 25, 2026

Sodium hydride → tert-Butyl 2-{[3-(bromomethyl)benzyl]oxy}ethylcarbamate

https://huagongshe.com/reaction/567844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzene, 1,3-bis(bromomethyl)-HCID 69373—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 2-{[3-(bromomethyl)benzyl]oxy}ethylcarbamateHCID 1847093474.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride (125 mg, 60% dispersion in mineral oil, 3.13 mmol) was added portionwise to an ice-cooled solution of tert-butyl 2-hydroxyethylcarbamate (500 mg, 3.10 mmol), and 1,3-bis(bromomethyl)benzene (8.2 g, 31.0 mmol) in tetrahydrofuran (15 ml), and the reaction stirred at 0° C. for an hour under a nitrogen atmosphere, then allowed to warm to room temperature. Saturated ammonium chloride solution (10 ml) was added, and the mixture partitioned between water and ethyl acetate, and the layers separated. The organic phase was then dried over MgSO4, and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using an elution gradient of ethyl acetate:pentane (15:85 to 75:25) to give the title compound as a colourless oil, (796 mg, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06180627B2
Source datasetuspto-grants-2001_01
ORD IDord-73fc043aabb942a686d71412f3c6aef9
Source noteuspto-grants-2001_01