HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 13064229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 4-Cyanophenol | HCID 13019 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2,6-Bis(chloromethyl)-4-fluorophenol | HCID 21162832 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 13064229 | HCID 13064229 | 3% |
Reaction Steps
p-Cyanophenol (19.4 g) and 2,6-bis(chloromethyl)-4-fluorophenol (17.0 g) were dissolved in nitrobenzene (250 ml) at 20°. The solution was cooled to 10° and crushed aluminium chloride (anhydrous 65 g) was added in 5 g portions over two hours. During the addition the temperature was maintained at 10°-12°. Stirring was continued at 20° for 14 hrs. The viscous black mixture was poured onto a vigorously stirred mixture of ice (2 l) and dichloro methane (2 l). The organic solvent layer was dried, dichloro methane and nitrobenzene removed by vacuum distillation and the residual tar passed through a silica column. The product, 2,6-bis(5-cyano-2-hydroxybenzyl)-4-fluorophenol (mp 222°) was obtained in 3% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04163801 |
| Source dataset | uspto-grants-1979_08 |
| ORD ID | ord-16ea062f75bb4991949b695f978a8f73 |
| Source note | uspto-grants-1979_08 |