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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565008Generated: October 28, 2026

Ethyl Acetate → tert-Butyl [4-(hydroxymethyl)benzyl]carbamate

https://huagongshe.com/reaction/565008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-(Tert-butoxycarbonylaminomethyl)benzoateHCID 6950640—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl [4-(hydroxymethyl)benzyl]carbamateHCID 279481375.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 1.40 g (36.8 mmol) of lithium aluminum hydride in 150 ml of tetrahydrofuran was stirred at 0° C. A solution of 13.0 g (49.0 imol) of 4-(tert-butoxycarbonylaminomethyl)benzoate in 50 ml of tetrahydrofuran was dropwise added slowly to the suspension. After completion of the dropwise addition, the solution was heated to reflux for 2 hours and then cooled to 0° C. After 20 ml of 50% tetrahydrofuran was dropwise added to the reaction mixture, 100 ml of ethyl acetate was added thereto. Insoluble matters were filtered off and the resulting filtrate was concentrated under reduced pressure. The concentrate was isolated and purified by silica gel column chromatography to obtain 8.80 g (75.7%) of 4-(tert-butoxycarbonylaminomethyl)benzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169107A
Source datasetuspto-grants-2001_01
ORD IDord-7e1e0045802f40348088c1580019fd3c
Source noteuspto-grants-2001_01