HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1-Chloro-4-{[2-(chloromethyl)phenyl]sulfanyl}-2-methoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | {2-[(4-Chloro-3-methoxyphenyl)sulfanyl]phenyl}methanol | HCID 12374605 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Chloro-4-{[2-(chloromethyl)phenyl]sulfanyl}-2-methoxybenzene | HCID 12374608 | 85% |
Reaction Steps
Thionyl chloride (6.5 g) is added dropwise to a stirred mixture of the alcohol from the preceding preparation (11.2 g) and pyridine (4.0 g) at 10°-20° C. The mixture is stirred at room temperature for 3 hours and, after standing overnight, for one additional hour at 30°-40° C. The cooled mixture is decomposed by dropwise addition of water (20 ml) and the product extracted with benzene. The work-up of the extract, followed by crystallization of the crude residue from a small volume of hexane, yields 10.2 g (85%) of 2-(4-chloro-3-methoxyphenylthio)benzyl chloride which in the pure state melts at 57°-59° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238611 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-0f3014e39cd84df6a31391a9025240a1 |
| Source note | uspto-grants-1980_12 |