HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667359Generated: October 25, 2026
Ethyl 2-methylacetoacetate → 5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid
https://huagongshe.com/reaction/1667359
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl 2-methylacetoacetate | HCID 701 | — |
| Reactant | 1,4-Butane sultone | HCID 15411 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acid | HCID 58084006 | 122.6% |
Reaction Steps
Ethyl 2-methylacetoacetate (43.2 g) in N,N-dimethylformamide (25 ml) was added to a suspension of sodium hydride (12.0 g of 60% NaH in mineral oil) in N,N-dimethylformamide (100 ml), dropwise with ice-bath cooling. This mixture was allowed to warm to ambient temperature for 30 mins before re-cooling. 1,4-butanesultone (40.8 g) in N,N-dimethylformamide (25 ml) was then added dropwise. The final mixture was heated at 50° C. for 18 hrs, then quenched with 50 ml of water. The solvent was evaporated under vacuum; the residue was partitioned between water and diethyl ether. The aqueous layer was collected, washed with fresh diethyl ether and evaporated under vacuum; final drying was under high vacuum over phosphorus pentoxide. A yield of 103 g of 5-(ethoxycarbonyl)-5-methyl-6-oxoheptane-1-sulfonic acid was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08044203B2 |
|---|
| Source dataset | uspto-grants-2011_10 |
|---|
| ORD ID | ord-a84c320341604e82bcceda72e086f20b |
|---|
| Source note | uspto-grants-2011_10 |
|---|