Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946414Generated: November 3, 2026

Bromomethylcyclopropane → HCID 59547832, compound

https://huagongshe.com/reaction/1946414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethylcyclopropaneHCID 81503—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 59547881HCID 59547881—
SolventDimethyl SulfoxideHCID 679—
SolventMethanolHCID 887—
ProductHCID 59547832HCID 59547832—

Reaction Steps

To a solution of 2,6-difluoro-N-(1-{[5-hydroxy-2-(trifluoromethyl)phenyl]methyl}-1H-pyrazol-3-yl)benzamide (for a preparation see Intermediate 42)(75 mg, 0.189 mmol) in DMSO (1 ml) was added potassium t-butoxide (23 mg, 0.205 mmol, Aldrich). The solution was stirred at ambient temperature for 5 min. To the solution was added (bromomethyl)cyclopropane (0.023 ml, 0.245 mmol, Alfa Aesar) and the mixture stirred overnight at ambient temperature under nitrogen. The solution was diluted with methanol (1 ml) and purified by MDAP on Sunfire C18 column (Method B) using Acetonitrile-Water with a Formic acid modifier. The solvent was evaporated in vacuo to give the title compound as a white solid (36 mg); LCMS: (System 4) MH+=452, tRET=3.18 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399436B2
Source datasetuspto-grants-2013_03
ORD IDord-dacd389ab6ed4d2397edd04bbf501f2e
Source noteuspto-grants-2013_03