HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085247Generated: October 27, 2026
Water → 2-(Benzylthio)-N,N-dimethylnicotinamide
https://huagongshe.com/reaction/1085247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | 2-chloro-N,N-dimethylpyridine-3-carboxamide | HCID 10965214 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Benzylthio)-N,N-dimethylnicotinamide | HCID 11086903 | 37.9% |
Reaction Steps
A solution of 25.0 g (223 mmol) of potassium t-butoxide in 100 ml of dimethylformamide was cooled to 0° C. and 22 ml (186 mmol) of benzyl mercaptan added dropwise at 0° C. After addition was complete, the reaction mixture was allowed to warm to 25° C. and stirred at this temperature for 15 minutes. The reaction mixture was then re-cooled to 0° C. and 34.0 g (186 mmol) of N,N-dimethyl-2-(chloro)-3-pyridinecarboxamide added in one portion. After an exotherm to 50° C, the mixture was heated at 80° C. for 1.5 hour. The mixture was cooled, poured into 100 ml of water and extracted with ether. The combined organic extracts were washed twice with water, then brine and dried over sodium sulfate. Concentration gave 19.2 g of a viscous yellow oil. IR (Nujol) 1640 (CONMe2) cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008393 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-1b0d6ea7a6d04824b62c3017c7206896 |
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| Source note | uspto-grants-1991_04 |
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