HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 3-Chloromethyl-4-(4-methyl-phenoxy)-toluene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 54261585 | HCID 54261585 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Chloromethyl-4-(4-methyl-phenoxy)-toluene | HCID 22767925 | — |
Reaction Steps
36.5 Ml. of thionyl chloride are added dropwise at 10°-15° C. with stirring and cooling with ice to a solution of 110 g. of 2-(4-methyl-phenoxy)-5-methyl-benzyl alcohol in 78 ml. of pyridine. The mixture is stirred for an additional 1 hour at 10° C. and then diluted with 200 ml. of benzene. Then, 200 ml. of water are carefully added dropwise with ice-cooling. The aqueous phase is separated and the organic phase washed successively with dilute hydrochloric acid, water and saturated sodium bicarbonate solution. The aqueous phases are each extracted once more with benzene. The combined benzene extracts are dried over sodium sulfate and evaporated to dryness in vacuo and there is obtained 3-chloromethyl-4-(4-methyl-phenoxy)-toluene as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04100173 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-bf103cfe1726442eb7d94744c3cbeb76 |
| Source note | uspto-grants-1978_07 |