HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 67119342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67119374 | HCID 67119374 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67119342 | HCID 67119342 | 71% |
Reaction Steps
After thionyl chloride (4 ml) was added to a solution of (2-ethyl-4′-methoxy-1,1′-biphenyl-3-yl)methanol (4.39 g, 17.9 mmol) obtained in Example (90-3) in methylene chloride (18 ml) under ice-cooling, the mixture was stirred at room temperature for 7 hours. The residue obtained by removing the solvent under reduced pressure was diluted with ethyl acetate and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The solvent was removed under reduced pressure to give 3′-(chloromethyl)-2′-ethyl-1,1′-biphenyl-4-yl methyl ether (3.32 g, yield: 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07923573B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-130fbbe17d4943a09237778bbd7a064f |
| Source note | uspto-grants-2011_04 |