HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 5-Chlorocarbonylphthalide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,3-Dihydro-1-oxoisobenzofuran-5-carboxylic acid | HCID 78517 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 5-Chlorocarbonylphthalide | HCID 9815555 | — |
Reaction Steps
5-Carboxyphthalid (53 g, 0.3 mole) was suspended toluene (200 mL) and thionylchloride (44 g, 0.6 mole). N,N-dimethylformamide (DMF) (1 mL) was added and the mixture was heated at reflux temperature for 3 hours. The mixture was cooled to room temperature and n-heptane was added (200 ml). The crystals formed were collected and washed with heptane (100 mL). Yield 52 g, 88%. DSC onset: 131° C. 1H NMR (CDCl3, 500 MHz): 5.47 (2H, s), 8.06 (1H, d , J=7.5 Hz), 8.28(1H, d, J=7.5 Hz), 8.3(1H, s). 13C NMR (CDCl3, 125 MHz): 69.4, 125.1, 126.1, 131.1, 131.6, 137.8, 146.6, 167.4, 169.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06392060B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-1cec08ce802f4e529f3a8d2151a5738c |
| Source note | uspto-grants-2002_05 |