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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284543Generated: October 29, 2026

Ethyl Acetate → 1-(4-Tert-butylphenyl)-3-(3-hydroxypropyl)urea

https://huagongshe.com/reaction/2284543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-Amino-1-propanolHCID 9086—
Reactant1-Tert-butyl-4-isocyanatobenzeneHCID 2735695—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product1-(4-Tert-butylphenyl)-3-(3-hydroxypropyl)ureaHCID 53520686110%

Reaction Steps

A solution of 3-amino-1-propanol (0.180 mL, 2.36 mmol) in diethylether (15 mL) was cooled at 0° C. and treated dropwise with 1-tert-butyl-4-isocyanatobenzene (0.400 mL, 2.25 mmol). The reaction mixture was allowed to slowly warm to room temperature. After 16 h the reaction was found to be complete by TLC (100% ethyl acetate) The reaction mixture was diluted with 10 mL portions of CH2Cl2 and Et2O and washed with 15 mL portions of H2O, 0.5N HCl and brine and dried over Na2SO4. The organic phase was filtered and concentrated to yield a colorless viscous oil which was dissolved in PhCH3, concentrated and placed under high vac overnight to yield the title compound (600 mg, 110%) as a colorless viscous oil: MS (ESI+) for C14H22N2O2 m/z 251.0 (M+H)+; (ESI−) for C14H22N2O2 m/z 249.3 (M−H)−; HPLC purity 98% (ret. time, 3.43 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145438B2
Source datasetuspto-grants-2015_09
ORD IDord-6e00f57d6d034699bd19fb25392f0114
Source noteuspto-grants-2015_09