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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640389Generated: November 1, 2026

Hydrochloric Acid → HCID 178477613, compound

https://huagongshe.com/reaction/1640389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantPotassium CyanideHCID 9032—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-Chloro-3-ethylsulfinyl-2-methylbenzoic acidHCID 66738909—
ReactantHCID 178429390HCID 178429390—
CatalystAcetone CyanohydrinHCID 6406—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178477613HCID 178477613—

Reaction Steps

128 mg (1.14 mmol) of 5-hydroxy-1,3-dimethylpyrazole were added to 270 mg (purity 95% by weight; 1.04 mmol) of 4-chloro-3-ethylsulfinyl-2-methylbenzoic acid in 20 ml of dichloromethane (CH2Cl2). 239 mg (1.24 mmol) of 1-(3′-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride were added, and the mixture was stirred at RT for 16 h. For work-up, 3 ml of 1M HCl were added, and the organic phase was freed from the solvent. 210 mg (2.07 mmol) of triethylamine, 10 drops of acetone cyanohydrin and a spatula tip of potassium cyanide were added to the residue in 20 ml of acetonitrile. The reaction mixture was stirred at RT for 16 h and then freed from the solvent. The residue was stirred at RT with 25 ml of a mixture of aqueous saturated sodium bicarbonate solution and diethyl ether for 10 min. The phases were separated, and the aqueous phase was acidified with dilute HCl and then extracted with CH2Cl2. The organic phase was freed from the solvent and the residue was then purified chromatographically. This gave 100 mg of clean product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114816B2
Source datasetuspto-grants-2012_02
ORD IDord-e20a6497e3d745b0bdf0ba47cc0e47f8
Source noteuspto-grants-2012_02