HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → alpha-Chloro-5-methyl-2-nitrotoluene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (5-Methyl-2-nitrophenyl)methanol | HCID 568847 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | alpha-Chloro-5-methyl-2-nitrotoluene | HCID 2724031 | — |
Reaction Steps
The above reaction product obtained in step (a) is mixed with 600 ml of benzene and 60 ml of thionyl chloride, and left to stand for 18 hours at room temperature. The reaction solution is concentrated and subsequently partitioned between benzene and ice-water. After the organic phase is washed, dried and evaporated, the heading compound remains as an orange, semi-crystalline crude product, which is used in step (c) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04372956 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-dafb066447b244b1a73620f05b30c1e3 |
| Source note | uspto-grants-1983_02 |