HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → Benzene, (chloromethyl)phenoxy-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Phenoxybenzyl alcohol | HCID 3660111 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Benzene, (chloromethyl)phenoxy- | HCID 169302 | 106.1% |
Reaction Steps
Into a 1 liter round bottom flask equipped with a stirrer, a condenser, a thermometer and an addition funnel are charged 25 g (0.125 mole) of o-phenoxybenzyl alcohol and 250 ml of benzene. Thionyl chloride (18.0 g, 0.15 mole) is added dropwise at room temperature. After the addition, the reaction mixture is heated to reflux for 2 hours. Solvent is then evaporated under vacuum to give 29 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05192783 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-2e6b1368490945298faa6c94782a96b4 |
| Source note | uspto-grants-1993_03 |