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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217260Generated: October 26, 2026

Water → 5-(1-Methylthioethyl)-2-pentafluoroethylpyridine

https://huagongshe.com/reaction/217260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium AcetateHCID 517165—
Reactant(1E)-1-ethoxy-4,4,5,5,5-pentafluoropent-1-en-3-oneHCID 5906496—
Reactant1-((E)-3-methylthiobut-1-enyl)pyrrolidineHCID 44185543—
SolventDiethyl EtherHCID 3283—
Product5-(1-Methylthioethyl)-2-pentafluoroethylpyridineHCID 5921860212%

Reaction Steps

(E)-1-Ethoxy-4,4,5,5,5-pentafluoropent-1-en-3-one (1.09 g, 5 mmol) in anhydrous ethyl ether (5 mL) was treated with 1-((E)-3-methylthiobut-1-enyl)pyrrolidine (0.85 g, 5 mmol) in 2 mL dry ether at −15° C. over a period of 5 min and the reaction was continued for 20 min. Then the temperature was allowed to rise to room temperature and the reaction continued for 3 h. The solvent was removed under reduced pressure and the residue re-dissolved in anhydrous DMF (5 mL). Ammonium acetate (0.58 g, 7.5 mmol) was added and the mixture stirred at room temperature over a weekend. Water was added and mixture extracted with ether three times. The combined organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, concentrated, and purified on silica gel eluted with 8% EtOAc in hexane (v/v) to give 0.16 g of the desired 5-(1-methylthioethyl)-2-pentafluoroethylpyridine (A) as brownish colored oil in 12% yield. GC-MS: mass calcd for C10H11F2N3S [M]+ 271. Found 271.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193364B2
Source datasetuspto-grants-2012_06
ORD IDord-202eeafc5cdc4efe81857cfc3ec0267e
Source noteuspto-grants-2012_06