HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207548Generated: November 1, 2026
Dimethylcarbamoyl Chloride → HCID 66718480, compound
https://huagongshe.com/reaction/2207548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | HCID 66718352 | HCID 66718352 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66718480 | HCID 66718480 | — |
Reaction Steps
To a stirred solution of 2-(4-hydroxytetrahydropyran-4-yl)pyridine-N-oxide (3.69 g, 18.91 mmol) in anhydrous dichloromethane was added dimethylcarbamoyl chloride (3.05 g, 28.4 mmol) and trimethylsilylcyanide (2.82 g, 28.4 mmol). The mixture was stirred for sixty hours at 40° C., after which time further aliquots of dimethyl carbamoyl chloride (3.05 g, 28.4 mmol) and trimethylsilylcyanide (2.82 g, 28.4 mmol) were added. After stirring at 40° C. for a further 24 hours, sodium carbonate solution (50 mL, 2 M aqueous solution) was added and the mixture stirred overnight. The resultant mixture was filtered and the layers partitioned. Sodium carbonate solution (50 mL, 2 M aqueous solution) was again added to the organic phase and stirred overnight. After separation of the phases, the organic layer was blown down at ambient temperature to give the title compound as a brown oil which was used in the next step without further purification; LC-MS Retention time 1.62 min, (M+H)+ 205.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09376443B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-59f2ac9e1d294dc3a42044e151f896d5 |
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| Source note | uspto-grants-2016_06 |
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