HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579407Generated: October 30, 2026
Ethyl 2-methylacetoacetate → Diethyl 2-acetyl-2-methyloctanedioate
https://huagongshe.com/reaction/579407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Reactant | 2-Methylpropan-2-olate | HCID 4574913 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Diethyl 2-acetyl-2-methyloctanedioate | HCID 22266834 | 72,751.203% |
Reaction Steps
A mixture of 13.4 g (0.12 mol) of potassium tert-butoxide and 100 g of tert-butanol was stirred and heated until the tert-butoxide totally dissolved. The solution was cooled to about 50° C. and 17 g (0.12 mmol) of ethyl 2-methylacetoacetate was added dropwise. Ethyl-6-bromohexanoate (30 g, 0.13 mmol) was then added dropwise and the reaction mixture was stirred and refluxed for 5 hours. The mixture was filtered and the solvent was removed under reduced pressure. The residue was partitioned between 1M HCl and chloroform. The organic layer was dried over magnesium sulfate and purified on silica gel using 1:10 ethyl acetate/hexane as the eluent to yield 25 g (75%) of diethyl 2-acetyl-2-methyloctanedioate (3) as yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09040721B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-db0bca3c94274489840839d5a6b08767 |
|---|
| Source note | uspto-grants-2015_05 |
|---|