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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673539Generated: October 29, 2026

Hydrochloric Acid → Tert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoate

https://huagongshe.com/reaction/1673539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(1,1'-Biphenyl)-3-carboxylic acidHCID 12854—
ReactantOxalyl chlorideHCID 65578—
ReactantTert-butyl 2-amino-4-phenoxybenzoateHCID 58508592—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoateHCID 673442706.6%

Reaction Steps

4.0 mL of methylene chloride, 0.015 mL of N-dimethylformamide and 0.050 mL of oxalyl chloride were added to 99 mg of 3-biphenylcarboxylic acid at room temperature sequentially and stirred at the same temperature for 20 minutes. 0.16 mL of triethylamine and 0.13 g of tert-butyl 2-amino-4-phenoxybenzoate were added to the reaction mixture at room temperature sequentially and stirred at the same temperature for 10 minutes. Ethyl acetate and 1.0 mol/L hydrochloric acid 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 14 mg of tert-butyl 2-(biphenyl-3-carboxamido)-4-phenoxybenzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-806b55725c3c45abbd4b065f9640584e
Source noteuspto-grants-2011_08