Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | HCID 54209632 | HCID 54209632 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | HCID 86760890 | HCID 86760890 | — |
Reaction Steps
1.46 mL (0.0174 mol) of chloroacetone are added to 1.5 g (0.0174 mol) of lithium bromide in 10 mL of acetone and the medium is stirred at room temperature for 15 minutes and then 1.5 g (0.00828 mol) of methyl 6-(methoxymethyl)nicotinate are added and the medium is heated under reflux overnight. 1.5 g (0.0174 mol) of lithium bromide and 1.46 mL (0.0174 mol) of chloroacetone are added to the reaction medium and the medium is kept under reflux for 5 hours. The medium is evaporated to dryness and the residue obtained is taken up in a dichloromethane-methanol (9-1) mixture. The insoluble material obtained is filtered and then 4.62 mL (0.033 mol) of triethylamine are added to the filtrate and the medium is stirred at room temperature for one hour. The reaction medium is concentrated. The residue obtained is taken up in toluene and the product is purified by filtration on a silica bed, eluting with toluene. After evaporation, 450 mg of a yellow solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07553845B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-17d230eb6d8246799e191363c680e04c |
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| Source note | uspto-grants-2009_06 |
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