HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Pentanedioic acid, 2,4-dimethyl-, monomethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Methylglutaric anhydride | HCID 77828 | — |
| Reactant | dihydro-3-methyl-2H-pyran-2,6(3H)-dione | HCID 3015571 | — |
| Reactant | Methyl 5-chloro-4-methyl-5-oxopentanoate | HCID 13192898 | — |
| Reactant | Methyl 4-chloro-3-methyl-4-oxobutanoate | HCID 14403282 | — |
| Product | Pentanedioic acid, 2,4-dimethyl-, monomethyl ester | HCID 549975 | — |
Reaction Steps
The starting materials for said compounds 1, 2, 4, 6, 11 and 12 are the 3-carbomethoxy-2-methylpropanoyl chloride, 2-methylglutaric anhydride, 4-carbomethoxy-2-methylbutanoyl chloride, 3-methylglutaric anhydride and the erythro or threo 4-carbomethoxy-4-(2-phenethyl)-2-methylbutanoyl chloride respectively. That of compound 8 and 9 may be prepared as follows: The solution of 6.0 of meso-2,4-dimethylglutaric acid anhydride [J. Am. Chem. Soc. 77, 1862 (1955)] in 4 ml of methanol is refluxed for one hour and evaporated, to yield the erythro 4-carbomethoxy-2,4-dimethylbutanoic acid. It is converted into the acid chloride by refluxing it with 10.9 g of oxalyl chloride in 50 ml of methylene chloride for 2 hours, and evaporating said mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04479963 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-6c1697f0a648407e8ce97bd6d40d4f9f |
| Source note | uspto-grants-1984_10 |