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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397645Generated: October 29, 2026

Thionyl Chloride → HCID 20321559, compound

https://huagongshe.com/reaction/2397645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 20321543HCID 20321543—
SolventDichloromethaneHCID 6344—
ProductHCID 20321559HCID 20321559—

Reaction Steps

The solution of 7.8 g of 3-[4-chloro-2-(2-chloro-αmethoxy-benzyl)-phenyl]-2-methylpyrazole-4-carboxylic acid in 75 ml of methylene chloride and 6.7 diisopropyl ethylamine is stirred in an ice bath and 4.7 ml of thionyl chloride are added. The mixture is refluxed for 40 minutes, cooled and washed with ice-water. The organic layer is dried, evaporated and the residue taken up in 65 ml of tetrahydrofuran and the solution saturated with ammonia. After stirring at 25° for 16 hours, the mixture is diluted in diethyl ether, washed with water and brine, dried and evaporated. The residue is dissolved in 300 ml of diethyl ether and the solution refluxed for 16 hours with 2 g of lithium aluminum hydride. After destroying the excess reagent and filtering off the precipitate, the filtrate is washed with diluted hydrochloric acid. The acidic layer is basified with aqueous sodium hydroxide and extracted with methylene chloride. The extract is dried, evaporated, the residue taken up in ethyl acetate and the solution acidified with hydrogen chloride, to yield the 3-[4-chloro-2-(2-chloro-α-methoxy-benzyl)-phenyl]-4-aminomethyl-2-methylpyrazole hydrochloride melting at 260°-262°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022800
Source datasetuspto-grants-1977_05
ORD IDord-a4c1ae3e97fd406f97c9069b0c6fc93b
Source noteuspto-grants-1977_05