HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 13826416, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13826415 | HCID 13826415 | — |
| Product | HCID 13826416 | HCID 13826416 | — |
Reaction Steps
(2,4,7-Trichloronaphthalen-1-yl)methanol (1.0 g, 3.8 mmoles) was added portionwise to thionyl chloride (10 ml) with cooling (ice bath). The reaction mixture was stirred at room temperature for 30 minutes and at reflux for 2 hours and then concentrated to dryness in vacuo. The oily residue was taken up in methylene chloride and the solution dried over MgSO4. The solution was filtered and concentrated in vacuo to give 1.0 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654363 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-e98f61805c684a1b8fd945bb0224af58 |
| Source note | uspto-grants-1987_03 |