HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → Dimethyl 3-phenylthiocyclobutane-1,2-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Phenyl Vinyl Sulfide | HCID 74572 | — |
| Reactant | Dimethyl maleate | HCID 5271565 | — |
| Reactant | Ethyl aluminium dichloride | HCID 16686341 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dimethyl 3-phenylthiocyclobutane-1,2-dicarboxylate | HCID 86746186 | — |
Reaction Steps
To a solution of dimethyl maleate (0.50 mL, 4 mmol) and phenyl vinyl sulfide (0.52 mL, 4 mmol) in 17 mL of 1,2-dichloroethane under nitrogen atmosphere, was added 1 equivalent (4 mL of a 1 M solution in hexane) of ethylaluminum dichloride. The resultant solution was heated at 85° C. for 18 h and then diluted with 75 mL of methylene chloride. The methylene chloride solution was washed three times with saturated aqueous ammonium chloride and once with brine, dried over anhydrous sodium sulfate, filtered and concentrated to give 0.98 g of the title compound; EI-MS, m/e (rel intensity): 280 (M+, 14), 136 (100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05246931 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-cfd97c6b760d447ab41eb374f30d7b03 |
| Source note | uspto-grants-1993_09 |