HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-Bromopyrimidine-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Bromopyrimidine-2-carboxylic acid | HCID 16462970 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Bromopyrimidine-2-carbonyl chloride | HCID 59674657 | 97.6% |
Reaction Steps
Oxalyl chloride (1.45 g, 11.1 mmol) was added to a suspension of 5-Bromo-pyrimidine-2-carboxylic acid (1.5 g, 7.4 mmol) in dichloromethane (50 ml) at room temperature followed by 1-2 drop of dimethylformamide. The reaction mixture was stirred under nitrogen for 2 hours LCMS in methanol indicated the presence of the methyl ester and some acid. Dimethylformamide (0.2 ml) was added to the reaction mixture and all of the acid dissolved after 30 minutes. LCMS showed corresponding methyl ester and no starting material peak was observed. The solvent was removed and dried in vacuo to afford the crude 5-Bromo-pyrimidine-2-carbonyl chloride (1.6 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735396B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-bedf0140362345e0932336ddd464982c |
| Source note | uspto-grants-2014_05 |