HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328232Generated: October 29, 2026
Dimethylcarbamoyl Chloride → HCID 21444460, compound
https://huagongshe.com/reaction/328232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3,5-Dimethyl-4-[(pyridin-2-yl)sulfanyl]phenol | HCID 21444456 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21444460 | HCID 21444460 | — |
Reaction Steps
To a stirred suspension of 240 mg. of sodium hydride in 20 ml. of dry tetrahydrofuran is added a solution of 2.31 g. of 3,5-dimethyl-4-(2-pyridylthio)phenol in 30 ml. of dry tetrahydrofuran. After the effervescence has subsided, a solution of 1.1 g. of N,N-dimethylcarbamoyl chloride in 10 ml. of dry tetrahydrofuran is added dropwise. The reaction mixture is stirred at ambient temperature for 16 hours, and then under reflux for 4 hours. The reaction mixture is cooled to room temperature, and then diluted with an excess of water. The product is extracted into ethyl acetate. The ethyl acetate is washed with water, dried using anhydrous magnesium sulfate, and then evaporated in vacuo to give crude 3,5-dimethyl-4-(2-pyridylthio)phenyl N,N-dimethylcarbamate. The crude product can be purified further by recrystallization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04016278 |
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| Source dataset | uspto-grants-1977_04 |
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| ORD ID | ord-39913770e708484b8c8abff61f6646fd |
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| Source note | uspto-grants-1977_04 |
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