HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22226281, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | HCID 53675890 | HCID 53675890 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22226281 | HCID 22226281 | — |
Reaction Steps
2.4 g of 1-bromomethylcyclopropylketone and 5.8 cm3 of pyridine are introduced into a three-necked flask containing 40 cm3 of ethanol and then the mixture is heated for 2 hours under reflux. After concentrating to dryness at 40° C. under reduced pressure (2.7 kPa), the residue is taken up in twice 30 cm3 of diethyl ether. After filtration, washing with diethyl ether, the precipitate is dried under reduced pressure (90 Pa) to give 3.4 g of 1-cyclopropylcarbonylmethylpyridinium bromide in the form of a cream-coloured solid melting at 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06958383B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-6ec0a1952c9a4d36af72ff322339ff1e |
| Source note | uspto-grants-2005_10 |