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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957243Generated: October 31, 2026

Sodium Methoxide → HCID 15766881, compound

https://huagongshe.com/reaction/1957243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 19068742HCID 19068742—
SolventMethanolHCID 887—
ProductHCID 15766881HCID 1576688153.4%

Reaction Steps

A solution of 3.6 g (7.78 mmol) of 3-chloro-2-[4-chloro-3-bis-(methylsulfonyl)aminophenyl]-5-trifluoromethylpyridine (prepared as in Example 13) and 100 mg of sodium methoxide in 100 ml of methanol were stirred at 20°-25° C. for three hours. Then most of the methanol was distilled off under reduced pressure. The residue was taken up in dilute hydrochloric acid, after which the product was extracted three times with ethyl acetate. The combined organic phases were dried over sodium sulfate and concentrated. The oily residue was treated with ether/petroleum ether to afford 1.6 g (53%) of colorless crystals of melting point 133°-134° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783522
Source datasetuspto-grants-1998_07
ORD IDord-c696d3f6579e4693ae2d8debd2aac310
Source noteuspto-grants-1998_07