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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355809Generated: October 28, 2026

Benzocaine → Ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate

https://huagongshe.com/reaction/355809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant2-[2-(Benzyloxy)-5-bromophenyl]acetic acidHCID 3307011—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoateHCID 5447518942.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 2-benzyloxy-5-bromophenylacetic acid (3.2 g) in toluene (100 ml) was added thionyl chloride (1.0 ml) and DMF (3 drops ). The reaction was stirred at 80° C. for 1 hour and cooled to ambient temperature. ethyl 4-aminobenzoate (2.0 g) and triethylamine (2 ml) were added to the reaction mixture with stirring. After standing for 18 hours, the mixture was diluted with dichloromethane and washed with water, 1N HCl solution, water and sautrated aqueous NaHCO3 solution. The organic extract was dried (MgSO4), filtered and evaporated and the residue purified by trituration with diethyl ether to give ethyl 4-[2-benzyloxy-5-bromophenylacetamido]benzoate (2.0 g) mpt. 174°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834468
Source datasetuspto-grants-1998_11
ORD IDord-99db7a75acb44c3f8d1d80065c95b309
Source noteuspto-grants-1998_11