Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 17909374 | HCID 17909374 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 17909371 | HCID 17909371 | — |
Reaction Steps
7.6 g of 2-chloro-4,6-dimethylphenylmalonic acid according to Example (XXXV-1) were suspended in 22 ml of toluene and treated dropwise with 19.5 ml of thionyl chloride. The mixture was heated at 95° C. for 9.5 h, cooled and freed from the volatile constituents by passing argon through. The residues of thionyl chloride and the solvent were distilled off at 45° C. in a high vacuum. 6.6 g of 2-chloro-4,6-dimethylphenylchlorocarbonylketene were obtained as an oil which was slightly contaminated with 2-chloro-4,6-dimethylphenylacetyl chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251830B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-4875abda3625456383e5e571d1b8b3c8 |
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| Source note | uspto-grants-2001_06 |
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