Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 22336865 | HCID 22336865 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22336854 | HCID 22336854 | — |
Reaction Steps
30 g of 2-(2,4,5-trimethylphenyl)-malonic acid were suspended in 60 ml of toluene at 50 to 60° C. and 62.5 ml of thionyl chloride were added dropwise. The mixture was then heated at 90 to 100° C. for 15 hours. It was then cooled, the volatile constituents were driven off with an inert gas and the excess thionyl chloride was distilled off. 30.6 g of 2,4,5-trimethylphenylchlorocarbonyl ketene were isolated as the residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06511942B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-fd40cd57cab4475fa63cae1c6d83dcd5 |
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| Source note | uspto-grants-2003_01 |
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