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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414259Generated: November 1, 2026

Dimethylthiocarbamoyl chloride → 2-methoxy-N,N-dimethyl-2-(2-pyridyl)thioacetamide

https://huagongshe.com/reaction/1414259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylthiocarbamoyl chlorideHCID 27871—
Reactant2-(Methoxymethyl)pyridineHCID 253220—
ReactantBenzene etherHCID 22174802—
ReactantHCID 178506676HCID 178506676—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product2-methoxy-N,N-dimethyl-2-(2-pyridyl)thioacetamideHCID 15581959—

Reaction Steps

To 0.10 mole of phenyl lithium in 100 ml. of benzene/ether at 0° C. is added dropwise 10.6 g. (0.084 mole) of 2-(methoxymethyl)pyridine dissolved in 75 ml. of benzene. To this mixture is added dropwise 10.0 g. (0.081 mole) of N,N-dimethylthiocarbamoyl chloride in 100 ml. of benzene. The resulting mixture is stirred at room temperature overnight, then poured into 100 ml. of water and acidified. The organic phase is extracted once with dilute aqueous acid. The combined aqueous phases are extracted twice with ether, then made basic to about pH 10 and extracted three times with chloroform. The combined chloroform extracts are dried over magnesium sulfate and the solvent is removed by evaporation. The residue is chromatographed, then distilled in vacuo to give 2-methoxy-N,N-dimethyl-2-(2-pyridyl)thioacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001241
Source datasetuspto-grants-1977_01
ORD IDord-3061b312e1224f7f82a49ed558534e2a
Source noteuspto-grants-1977_01