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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639719Generated: October 30, 2026

Ethyl Acetate → 3-[(2-Methoxyethoxy)carbonylamino]benzyl alcohol

https://huagongshe.com/reaction/639719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-Methoxyethyl chloroformateHCID 69400—
Reactant3-Aminobenzyl alcoholHCID 80293—
SolventTetrahydrofuranHCID 8028—
Product3-[(2-Methoxyethoxy)carbonylamino]benzyl alcoholHCID 67347770—

Reaction Steps

To a solution of 15.0 g of 3-aminobenzyl alcohol in 120 ml of tetrahydrofuran was added dropwise a solution of 18 ml of 2-methoxyethyl chloroformate in 70 ml of tetrahydrofuran under ice-cooling. After stirred for 30 minutes under ice-cooling and then at room temperature for 30 minutes, additional 2 ml of 2-methoxyethyl chloroformate was added, and the mixture was stirred at room temperature for 1 hour. After ethyl acetate was added, the mixture was washed successively with an aqueous saturated sodium bicarbonate solution and then an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated to obtain 30.2 g of 3-[(2-methoxyethoxy)carbonylamino]benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691883B2
Source datasetuspto-grants-2010_04
ORD IDord-fade4e6a07bf4952974b2573a70727ec
Source noteuspto-grants-2010_04