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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247430Generated: October 26, 2026

3-Methoxybenzylamine → Tert-butyl 3-methoxybenzylcarbamate

https://huagongshe.com/reaction/2247430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzylamineHCID 21156—
ReactantTert-butyldicarbonateHCID 22064466—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-methoxybenzylcarbamateHCID 17870741—

Reaction Steps

3-Methoxybenzylamine (23 g) was dissolved in 150 ml of tetrahydrofuran, and a solution of 32 g of t-butyl dicarbonate in tetrahydrofuran (50 ml) was added thereto. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. The residue was dissolved in ethyl acetate and successively washed with 1N hydrochloric acid and brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated to give t-butyl N-(3-methoxybenzyl)carbamate. The resulting t-butyl N-(3-methoxybenzyl)carbamate was then dissolved in 250 ml of acetonitrile, 30 g of N-bromosuccinimide was added thereto under ice-cooling, the mixture was stirred at room temperature for 3 hours, and then the solvent was evaporated. The residue was dissolved in ethyl acetate and washed with water and then with brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by a silica gel column, to give 36 g of the title compound in the 2:1 hexane-diethyl ether fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687664B2
Source datasetuspto-grants-2010_03
ORD IDord-2af222adb7a2421da7b316307f4d258b
Source noteuspto-grants-2010_03