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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673502Generated: October 25, 2026

Oxalyl chloride → tert-butyl 2-((E)-3-(4-acetoxyphenyl)acrylamido)-4-phenoxybenzoate

https://huagongshe.com/reaction/1673502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantCinnamic acid, p-hydroxy-, acetateHCID 85857—
ReactantSodium BicarbonateHCID 516892—
ReactantTert-butyl 2-amino-4-phenoxybenzoateHCID 58508592—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Producttert-butyl 2-((E)-3-(4-acetoxyphenyl)acrylamido)-4-phenoxybenzoateHCID 67343538—

Reaction Steps

2.0 mL of methylene chloride, 3.9 μL of N,N-dimethylformamide and 0.094 mL of oxalyl chloride were added to 206 mg of 4-acetoxycinnamic acid at room temperature sequentially and stirred at the same temperature for 1 hour. The reaction mixture was added to a mixed solution of 86 mg of tert-butyl 2-amino-4-phenoxybenzoate, 3.0 mL of methylene chloride and 0.67 mL of triethylamine and stirred at room temperature for 1 hour. A saturated sodium hydrogen carbonate aqueous solution was added to the reaction mixture, and the organic layer was separated, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Trikonex Company, eluent; hexane; ethyl acetate=4:1] to obtain tert-butyl 2-((E)-3-(4-acetoxyphenyl)acrylamido)-4-phenoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-aaee3455ea144cc4a55c052e19c09dd0
Source noteuspto-grants-2011_08