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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774302Generated: October 31, 2026

Potassium Iodide → Tyclopyrazoflor

https://huagongshe.com/reaction/1774302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
ReactantN-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-3-((3,3,3-trifluoropropyl)thio)propanamideHCID 86700584—
SolventSulfolaneHCID 31347—
ProductTyclopyrazoflorHCID 86700627—

Reaction Steps

To 3-neck round bottomed flask (50 mL) was added sodium hydride (60% in oil, 0.130 g, 3.28 mmol) and sulfolane (16 mL). The gray suspension was stirred for 5 minutes then N-(3-chloro-1-(pyridin-3-yl)-1H-pyrazol-4-yl)-3-((3,3,3-trifluoropropyl)thio)propanamide (1.20 g, 3.16 mmol) dissolved in sulfolane (25 mL) was slowly added dropwise over 5 minutes. The mixture became a light gray suspension after 3 minutes and was allowed to stir for 5 minutes after which time ethyl bromide (0.800 mL, 10.7 mmol) and potassium iodide (0.120 g, 0.720 mmol) were added sequentially. The cloudy suspension was then allowed to stir at room temperature. The reaction was quenched after 6 hours by being poured drop-wise into cooled ammonium formate/acetonitrile solution (30 mL). The resulting orange colored solution was stirred and tetrahydrofuran (40 mL) was added. The mixture was assayed, using octanophenone as a standard, and found to contain 1.09 g (85%) of the desired product with a selectivity versus the retro-Michael-like decomposition product of 97:3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260396B2
Source datasetuspto-grants-2016_02
ORD IDord-4616fa7045b84acba0f2355591bc6e19
Source noteuspto-grants-2016_02