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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988345Generated: November 3, 2026

Ethyl Acetate → Tert-butyl N-[2-(2-hydroxyethyl)phenyl]carbamate

https://huagongshe.com/reaction/1988345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-(4-((Tert-butoxycarbonyl)amino)phenyl)acetic acidHCID 2824993—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl N-[2-(2-hydroxyethyl)phenyl]carbamateHCID 10752353—

Reaction Steps

4-(t-butoxycarbonylamino)-benzeneacetic acid (2.9 g, 11.4 mmoles) is dissolved in 10 ml of anhydrous THF at 0° C. and added to a suspension of LiAlH4 (0.52 g, 13.6 mmoles) in 30 ml of THF. The reaction mixture is agitated at ambient temperature for 1.5 hours. 50 ml of ethyl acetate then 20 ml of 2N soda are added to the medium. The expected product is extracted from the organic phase, which is then washed with 3 times 15 ml of water. The organic phase is dried and the solvent evaporated off under reduced pressure. Then the reaction product is purified on silica gel in a dichloromethane/methanol mixture (95/5). 1.1 g (40%) is thus obtained in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07553976B2
Source datasetuspto-grants-2009_06
ORD IDord-15658b37579c4aaeb998f5f218be48c6
Source noteuspto-grants-2009_06