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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673535Generated: October 31, 2026

Hydrochloric Acid → HCID 67344183, compound

https://huagongshe.com/reaction/1673535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Cyanobenzoic acidHCID 15875—
ReactantOxalyl chlorideHCID 65578—
ReactantTert-butyl 2-amino-4-phenoxybenzoateHCID 58508592—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 67344183HCID 67344183—

Reaction Steps

To 0.17 g of 3-cyanobenzoic acid were added 2.5 mL of methylene chloride, 0.015 mL of N,N-dimethylformamide and 0.095 mL of oxalyl chloride at room temperature sequentially and stirred at the same temperature for 30 minutes. The reaction mixture was added to a mixed solution of 3.0 mL of methylene chloride and 0.35 mL of triethylamine containing 0.26 g of tert-butyl 2-amino-4-phenoxybenzoate at room temperature and stirred at the same temperature for 10 minutes. Ethyl acetate, 1.0 mol/L hydrochloric acid and tetrahydrofuran were added to the reaction mixture. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; chloroform] to obtain 0.20 g of tert-butyl 2-(3-cyanobenzamido)-4-phenoxybenzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-2198e85dc7754ead8eec83327540eea3
Source noteuspto-grants-2011_08