Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nicotinic Acid | HCID 938 | — |
| Reactant | (Chloromethyl)sulfonyl chloride | HCID 77054 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bis(tetrabutylammonium) sulphate | HCID 11433187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Chloromethyl nicotinate | HCID 14608830 | 25.5% |
Reaction Steps
A mixture of nicotinic acid (200 mg, 1.6 mmol), sodium bicarbonate (540 mg, 6.4 mmol), and tetrabutylammonium sulfate (54 mg, 0.16 mmol) was dissolved in a mixture of 4 ml of dichloromethane and 4 ml of water, and cooled to 0° C. To this stirred mixture was added chloromethylchlorosulfone (165 μl, 1.6 mmol) in 1 ml of dichloromethane, and the mixture was allowed to warm to room temperature, stirring overnight. The organic layer was separated, washed with brine, dried over sodium sulfate, and concentrated under reduced pressure to a yellow oil, which was dissolved in dichloromethane and filtered through a silica plug. Removal of the solvent under reduced pressure provided chloromethyl pyridine-3-carboxylate (70 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143249B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-8946598f922f477e912ede868215ac44 |
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| Source note | uspto-grants-2012_03 |
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