HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 5-(2,2-dichlorovinyl)-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,2,8-trimethyl-4H-(1,3)dioxino(4,5-c)pyridine-5-carbaldehyde | HCID 15619946 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 5-(2,2-dichlorovinyl)-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine | HCID 20264048 | — |
Reaction Steps
To a well stirred ice-cooled mixture of 0.1 mole of triphenylphosphine and 0.1 mole of potassium t-butoxide in 250 ml. of heptane is added over thirty minutes a mixture of 0.1 mole of chloroform in 200 ml. of heptane. The resulting mixture is concentrated in vacuo at 15°-20° to a volume of about 100 ml. and a solution of 0.1 mole of 2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]-pyridine-5-carboxaldehyde in 250 ml. of heptane is added. The reaction mixture was heated at 40°-50° for 5 hours, then cooled, filtered, and concentrated in vacuo to give crude product. Chromatography on silica gel and elution with ether-petroleum ether (10-50%) gives pure 5-(2,2-dichlorovinyl)-2,2,8-trimethyl-4H-1,3-dioxino[4,5-c]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04546106 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-57e128a5a6c94a6084ef94f74f74c847 |
| Source note | uspto-grants-1985_10 |