HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 13235877, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 6-(3-Bromophenyl)pyridazin-3(2H)-one | HCID 12881647 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 13235877 | HCID 13235877 | — |
Reaction Steps
To 50 ml of dry benzene were added 2.51 g of 6-(3-bromophenyl)-3(2H)-pyridazinone, 0.45 g of paraformaldehyde and 1 ml of thionyl chloride, after which the mixture was heated under reflux for 1 hour. The mixture was then cooled and filtered, and the filtrate was evaporated to dryness under reduced pressure, to give 3.11 g of crude crystals of the desired Compound No. 5. These were recrystallised from a 4:1 by volume mixture of hexane and benzene, to give 2.0 g of pure Compound No. 5, in the form of white needles melting at 135°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04738961 |
| Source dataset | uspto-grants-1988_04 |
| ORD ID | ord-05aba5faa75549909a066ee6b8a41917 |
| Source note | uspto-grants-1988_04 |