HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 86584468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 86584469 | HCID 86584469 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86584468 | HCID 86584468 | — |
Reaction Steps
A mixture of 6.9 g (20 mmol) of methyl 2-chloro-3-(1′-hydroxy-2′,2′-dimethylethylaminocarbonyl)-4-methylsulfonylbenzoate and 5 ml of thionyl chloride was stirred for 6 hours at room temperature. The solution was diluted with 50 ml of dichloromethane and subsequently concentrated. The residue was dissolved in 20 ml of dichloromethane. The addition of cyclohexane resulted in a crystalline precipitate which was filtered off with suction and dried. This gave 6.4 g (88% of theory) of methyl 2-chloro-3-(1′-chloro-2′,2′-dimethylethylaminocarbonyl)-4-methylsulfonylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045465B1 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-bc2db9591b4c433d835ada54c0d1a16e |
| Source note | uspto-grants-2015_06 |