HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (5-Bromo-4-chloropyridin-2-yl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 5-Bromo-4-chloro-2-methylpyridine 1-oxide | HCID 13682778 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (5-Bromo-4-chloropyridin-2-yl)methanol | HCID 19791171 | — |
Reaction Steps
3.0 mL trifluoroacetic anhydride were added dropwise at 10° C. to 2.6 g (12 mmol) 5-bromo-4-chloro-2-methylpyridine-1-oxide in 30 mL DCM. The reaction mixture was stirred for 5 days at RT. After the addition of MeOH the reaction mixture was evaporated down, the residue was combined with 15% potassium carbonate solution and extracted several times with EtOAC. The combined organic phases were dried on sodium sulphate and evaporated down.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829006B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-3c280e930d3a4fb9aa6a1b2618d9a15a |
| Source note | uspto-grants-2014_09 |