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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214407Generated: October 31, 2026

Dichloromethane → HCID 21933564, compound

https://huagongshe.com/reaction/2214407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTert-Butyl nitriteHCID 10906—
ReactantTrifluoromethanesulfonic acidHCID 62406—
ReactantHCID 21933567HCID 21933567—
SolventPentaneHCID 8003—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 21933564HCID 2193356415.6%

Reaction Steps

First, 1.92 g of trifluoromethanesulfonic acid was added dropwise to a mixture of 2.54 g of 3-amino-2-(methoxycarbonyl)methylthiopyridine, 6 ml of 1,2-dimethoxyethane, and 2 ml of dichloromethane at −10° C. After stirring at the same temperature for 10 minutes, a solution of 1.59 g of t-butyl nitrite in 1 ml of 1,2-dimethoxyethane was added dropwise to the reaction mixture at −5° C. or lower. After stirring at the same temperature for 30 minutes, n-pentane was poured into the mixture. The lower one of the two layers separated was dissolved in 3 ml of acetic anhydride, and the solution was stirred at 50° C. to 70° C. for 1 hour. The reaction mixture was cooled to room temperature and then poured into water, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated. The residue was subjected to silica gel chromatography to give 0.48 g of 3-acetoxy-2-(methoxycarbonyl)methylthiopyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109148B2
Source datasetuspto-grants-2006_09
ORD IDord-9c3277c2cc394ed69917bcbd8bb477be
Source noteuspto-grants-2006_09