HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 23631899, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (5-Bromopyridin-2-yl)methanol | HCID 5200169 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23631899 | HCID 23631899 | — |
Reaction Steps
A mixture of (5-Bromo-pyridin-2-yl)-methanol (60 mg, 0.32 mmol) in dichloromethane (2 ml) was cooled in as ice bath. To the mixture was then added triethylamine (0.13 mL, 0.96 mmol) followed by methanesulfonyl chloride (0.05 mL, 0.64 mmol). The reaction mixture was stirred at room temperature for 2 hours. To the reaction mixture was added saturated aqueous sodium bicarbonate (5 mL). The organic phase was separated and the aqueous phase extracted further with dichloromethane (2×5 mL). The combined organic phase was washed with brine, dried over sodium sulfate and concentrated to give the product as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07485722B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-4a3e0bbcdc4746bfb6b15171314d9ff7 |
| Source note | uspto-grants-2009_02 |