HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414830Generated: October 26, 2026
Ammonium Chloride → 4,6,6-Trimethylheptan-2-one
https://huagongshe.com/reaction/1414830
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5,5-Trimethylhexanoic acid | HCID 90960 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4,6,6-Trimethylheptan-2-one | HCID 3016169 | — |
Reaction Steps
250 ml. of a ca. 2-M ethereal methyl lithium solution are added dropwise to 39.5 g. of 3,5,5-trimethylhexanoic acid in 250 ml. of absolute diethyl ether at such a rate that a slight reflux is maintained. After completion of the addition, the mixture is stirred at room temperature for 1.5 hours, then cooled in an ice bath and 100 ml. of saturated aqueous ammonium chloride solution are cautiously added dropwise with stirring. The mixture is filtered through diatomaceous earth and the two phases of the filtrate are separated. The aqueous phase is back-extracted once with diethyl ether and the ether solutions are washed successively with ammonium chloride solution, water and saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated. By distillation there is obtained pure 4,6,6-trimethyl-2-heptanone of boiling point 64°-67° C./12 mmHg; nD20 = 1.4258.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04002647 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-d5b9937cf68a414e89245b18a7282869 |
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| Source note | uspto-grants-1977_01 |
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