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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963149Generated: October 30, 2026

Ammonium Hydroxide → HCID 19080724, compound

https://huagongshe.com/reaction/963149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 19080749HCID 19080749—
SolventDichloromethaneHCID 6344—
ProductHCID 19080724HCID 19080724—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 22.5 g (91.6 mmol) of 5-chloro-1-ethyl-3-(trifluoromethyl)pyrazole-4-carboxylic acid and 45 mL of thionyl chloride was prepared and heated to reflux with stirring for 3 hours. The slurry became a dark orange solution. The excess thionyl chloride and other volatiles were removed by evaporation under reduced pressure to obtain a dark brown oil. This was taken up in 250 mL of dichloromethane and the resulting solution was cooled to about 0° C. and treated with 100 mL of concentrated ammonium hydroxide, which was added dropwise with stirring and cooling. When the addition was complete, the mixture was allowed to warm to ambient temperature and stir over a 2-hour period. The solids were collected by filtration and washed with water (3×50 mL). The solids that formed in the filtrate due to evaporation of the dichloromethane were collected in the same way. The combined solids were washed with water (2×100 mL) and were then suspended in water for 2 hours, recollected by filtration, and dried in an oven under reduced pressure. The white solid obtained was 18.4 g of the title compound melting at 15°-152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763359
Source datasetuspto-grants-1998_06
ORD IDord-466dfb22c7f54d4aa6a35a0c12d5bc6d
Source noteuspto-grants-1998_06