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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352585Generated: November 1, 2026

Benzyl Bromide → HCID 21913792, compound

https://huagongshe.com/reaction/1352585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium HydroxideHCID 14798—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
CatalystBenzyltrimethylammonium chlorideHCID 5963—
SolventDichloromethaneHCID 6344—
ProductHCID 21913792HCID 2191379294.8%

Reaction Steps

Benzyltrimethylammonium chloride (4.61 g, 24.8 mmol) was added to a mixture of tert-butyl 2-hydroxyethylcarbamate (40.0 g, 248 mmol), dichloromethane (600 mL), and 50% aqueous sodium hydroxide (400 mL). Benzyl bromide (29.5 mL, 248 mmol) was then added, and the reaction was stirred for three hours. Ice water was added (1 L), and the aqueous solution was extracted with chloroform (5×). The combined organic solutions were washed with water (2×) and brine (3×), dried over magnesium sulfate, filtered, and concentrated under reduced pressure. Upon concentration, a white precipitate formed, and the organic solution was washed again with water (3×100 mL). The combined washings were extracted with chloroform (3×50 mL). The combined organic solutions were washed with brine (3×50 mL), dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 59.1 g of tert-butyl 2-(benzyloxy)ethylcarbamate as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220758B2
Source datasetuspto-grants-2007_05
ORD IDord-0d4e2689ee2b45e7bee19d1e1a5c651d
Source noteuspto-grants-2007_05