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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990622Generated: October 31, 2026

1-Pyrrolidinecarbonyl chloride → HCID 18415666, compound

https://huagongshe.com/reaction/990622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Pyrrolidinecarbonyl chlorideHCID 70937—
ReactantHCID 178527384HCID 178527384—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 18415666HCID 1841566665%

Reaction Steps

To a solution of 0.12 g (0.45 mmol) 3-(bromodifluoromethylsulfonyl)-1,2,4-triazole, prepared as above, in 0.5 ml dry pyridine was added 0.07 g (0.54 mmol) pyrrolidine-1-carbonyl chloride and the mixture was agitated for 16 h at room temperature. The reaction mixture was then diluted with water and extracted with ether. The resulting organic layer was washed successively with dilute hydrochloric acid, water and saturated sodium bicarbonate solution, dried over MgSO4 and evaporated to give 0.1 g (65% yield) of the desired 3-(bromodifluoromethylsulfonyl)-1-(pyrrolidinocarbonyl)-1,2,4-triazole as a pale yellow oil: 1H NMR (CDCl3) δ(ppm) 9.1 (1H), 4.0 (2H), 3.7 (2H), 2.1 (4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06461997B1
Source datasetuspto-grants-2002_10
ORD IDord-a74cd095b8f44040af0ebf32a095d114
Source noteuspto-grants-2002_10