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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842155Generated: October 31, 2026

Sodium borohydride → HCID 10294562, compound

https://huagongshe.com/reaction/842155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 53786085HCID 53786085—
SolventMethanolHCID 887—
ProductHCID 10294562HCID 10294562—

Reaction Steps

To a suspension of 4-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-5-ethoxymethyleneamino-3-trifluoromethylpyrazole (1.0 g) in methanol (10 ml) stirred at room temperature was added sodium borohydride (0.17 g). After 2 hours an additional 0.17 g of sodium borohydride was added, and another 0.34 g added after 1 hours. One hour later the mixture was poured onto water (80 ml). The combined extracts were dried over anhydrous magnesium sulphate, filtered, and evaporated in vacuo. The white solid thus obtained was purified by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm−2) with dichloromethane as eluent, to furnish 4-cyano-5-methylamino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-trifluoromethylpyrazole as a white solid )0.6 g), m.p. 200-202° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06372774B1
Source datasetuspto-grants-2002_04
ORD IDord-437acebd07424a4f9dec7cf0c8e026e3
Source noteuspto-grants-2002_04