HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076375Generated: October 25, 2026
Dimethylthiocarbamoyl chloride → 2-methoxy-N,N-dimethyl-2-(2-pyridyl)thioacetamide
https://huagongshe.com/reaction/1076375
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | 2-(Methoxymethyl)pyridine | HCID 253220 | — |
| Reactant | Benzene ether | HCID 22174802 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-methoxy-N,N-dimethyl-2-(2-pyridyl)thioacetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03956494 |
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| Source dataset | uspto-grants-1976_05 |
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| ORD ID | ord-8dced8367e834f5994f43cd105609757 |
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| Source note | uspto-grants-1976_05 |
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