HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614869Generated: October 25, 2026
Acetyl chloride → 4-Carbomethoxy-2-methylbutanoic acid
https://huagongshe.com/reaction/614869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Methylglutaric Acid | HCID 12046 | — |
| Reactant | 4-Methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt | HCID 70583400 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Carbomethoxy-2-methylbutanoic acid | HCID 13192897 | — |
Reaction Steps
2-Methylglutaric acid (14.6 g.) and acetyl chloride (26 ml.) are heated in the steam bath for one hour. The mixture is concentrated to dryness in vacuo and the residue is evaporated twice from toluene. The residue is dissolved in methanol (4.7 ml.) and heated on the steam bath for one hour and concentrated to dryness. The residue is dissolved in a mixture of ether (17 ml.), dicyclohexylamine (16.7 ml.) and hexane (83 ml.). The crystalline salt is filtered off and the filtrate is concentrated to one third volume and chilled. The crystals are filtered and dried to yield 11.3 g. of 4-methoxycarbonyl-2-methyl butanoic acid dicyclohexylamine salt, m.p. 97°-99°. The salt is converted to the free acid by distribution between ethyl acetate and aqueous acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04146639 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-ab940557bcf1458186603e60133c664c |
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| Source note | uspto-grants-1979_03 |
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