HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → (2-Chlorophenyl)diphenylmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Benzene, 1-chloro-2-(trichloromethyl)- | HCID 16494 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | (2-Chlorophenyl)diphenylmethanol | HCID 298659 | — |
Reaction Steps
Into a flask, benzene (380 ml) was charged, and aluminum chloride (88 g) was suspended therein. A solution of o-chlorobenzotrichloride (138 g, 0.6 mole) in benzene (145 ml) was dropwise added thereto over 2 hours while keeping the temperature at 60° C. After the addition was completed, the mixture was refluxed for 2 hours. The reaction mixture was poured into water (600 ml), and the flask was washed with benzene (240 ml) and water (120 ml). The combined mixture was refluxed for 4 hours. The organic layer was separated, washed with water (400 ml), treated with charcoal (6 g) and filtered. Evaporation of the benzene filtrate gave 172.6 g of o-chlorophenyldiphenylmethanol as a crystalline mass. Yield, 97.7%. M.P., 88.5°-91.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04216333 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-8847892dd2684a0f8b0f2a3659b96da3 |
| Source note | uspto-grants-1980_08 |