Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436902Generated: October 30, 2026

HCID 178469914, compound → HCID 178519878, compound

https://huagongshe.com/reaction/436902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178469914HCID 178469914—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178519878HCID 178519878—

Reaction Steps

A solution of 12 g of ethyl-(4-chloro-phenyl-4-ethoxycarbonyl-pyrazole in 150 ml of tetrahydrofuran is cooled in an ice bath. Then 25 ml of a 1 molar solution of aluminum hydride triethylamine complex in benzene is added dropwise. After the addition, the ice bath is removed and the gelatinous mixture stirred at room temperature for 21/2 hours. Excess reagent is then destroyed by the dropwise addition of water followed by 30 ml of an aqueous 2N solution of sodium hydroxide. The layers are separated, the aqueous phase reextracted with ethyl acetate and the combined organic layers dried over anhydrous sodium sulfate. The recrystallization of the solid residue from hot ethyl acetate gives the 3-(4-chloro-phenyl)-4-hydroxymethyl-pyrazole, m.p. 149°-150°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04028381
Source datasetuspto-grants-1977_06
ORD IDord-596db95e7d204302a02a3a31a9678c64
Source noteuspto-grants-1977_06