HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(4-Chloro-3-methoxyphenylthio)-4-methoxybenzyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | {2-[(4-Chloro-3-methoxyphenyl)sulfanyl]-4-methoxyphenyl}methanol | HCID 12374912 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 2-(4-Chloro-3-methoxyphenylthio)-4-methoxybenzyl chloride | HCID 12374916 | — |
Reaction Steps
Thionyl chloride (40.5 g) is added dropwise at 10°-20° C. to a stirred solution of the alcohol from the preceding experiment (91 g) in pyridine (30 ml) and chloroform (30 ml) in the course of 1 hour. The mixture is stirred at room temperature for an additional hour, set aside for 48 hours, heated to 40° C. for 2 hours and decomposed with water. The product is isolated by extraction with benzene. The extract affords 86 g of crude oily 2-(4-chloro-3-methoxyphenylthio)-4-methoxybenzyl chloride which is used without purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238611 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-84f17eae1a7c4cad8ef8da7671a35bba |
| Source note | uspto-grants-1980_12 |