HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Diisopropyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzhydrol | HCID 7037 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phenylmalonic acid | HCID 75791 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 20472690 | HCID 20472690 | — |
Reaction Steps
Following the procedure of Goldman et al. (U.S. Pat. No. 3,773,757), phenylmalonic acid (72 g., 0.40 mole), thionyl chloride (52.4 g., 0.44 mole) and dimethylformamide (0.070 ml.) are mixed in diisopropyl ether and refluxed for 2 hours. The resulting solution of phenylmalonic acid-half acid chloride is cooled and stored under an inert atmosphere until use. Following a procedure analogous to that of Goldman et al., benzhydryl alcohol (73.6 g., 0.40 mole) is added to the half-acid chloride solution and the mixture again refluxed for 2 hours. The volume is reduced by half, providing a diisopropylether solution of 2-phenyl-2-benzhydryloxycarbonylacetyl chloride used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04348264 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-8492c9094a8b480ba4c844fbfdc97593 |
| Source note | uspto-grants-1982_09 |