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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-methylacetoacetateHCID 701—
Reactant1,4-Butane sultoneHCID 15411—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product5-Ethyloxycarbonyl-5-methyl-6-oxo-1-heptanesulfonic acidHCID 58084006122.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044203B2
Source datasetuspto-grants-2011_10
ORD IDord-a84c320341604e82bcceda72e086f20b
Source noteuspto-grants-2011_10