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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851867Generated: October 30, 2026

Hydrochloric Acid → HCID 23023856, compound

https://huagongshe.com/reaction/851867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMethyl 3-amino-2-chlorobenzoateHCID 15132848—
Reactant3-Cyano-4-(2-methylpropoxy)benzoic acidHCID 23023850—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23023856HCID 23023856—

Reaction Steps

Oxalyl chloride (889 mg, 7.0 mmol) was dropwise added to a solution of 3-cyano-4-isobutyloxybenzoic acid (767 mg, 3.5 mmol) in dichloromethane (10 mL) under cooling with ice. Subsequently, a catalytic amount of DMF was added. The mixture was then stirred for one hour at room temperature, heated under reflux for 3 hours, and placed under reduced pressure to distill the solvent off. Toluene was added to the residue and the solvent was distilled off under reduced pressure. THF (10 mL) was added to the residue. Further, a solution of methyl 3 amino-2-chlorobenzoate (497 mg, 2.68 mmol) and triethylamine (1.39 mL, 10 mmol) in THF (10 mL). The resulting mixture was stirred for 14 hours at room temperature, and toluene and aqueous 1M hydrochloric acid were added. The organic portion was taken out, washed with aqueous 1M hydrochloric acid and aqueous saturated sodium hydrogen carbonate, dried over anhydrous magnesium sulfate, and placed under reduced pressure to distill the solvent off.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253154B2
Source datasetuspto-grants-2007_08
ORD IDord-0338b59f463e49dba96a30b64fdeda9e
Source noteuspto-grants-2007_08