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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375113Generated: October 29, 2026

Acetic Acid → 4,4-Diacetyl-5-(ethoxycarbonyl)-heptanedioic acid diethyl ester

https://huagongshe.com/reaction/1375113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiethyl fumarateHCID 638144—
ReactantHexanoic acid, 4-acetyl-5-oxo-, ethyl esterHCID 2733934—
Catalyst1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventDiethyl EtherHCID 3283—
Product4,4-Diacetyl-5-(ethoxycarbonyl)-heptanedioic acid diethyl esterHCID 5878495353.6%

Reaction Steps

25.7 g of 4-acetyl-5-oxohexanoic acid ethyl ester and 0.3 g of 1,8-diazabicyclo-[5.4.0]-undec-7-ene were mixed, and 35 g of fumaric acid diethyl ester was added at room temperature over 40 minutes. After stirring for 24 hours, the amount of 1,8-diazabicyclo-[5.4.0]-undec-7-ene was doubled and stirring continued until conversion was complete. 0.5 g of acetic acid and 50 ml of diethyl ether were added, and the solution was extracted with an aqueous potassium carbonate solution and water. Fractional distillation of the dry organic layer yielded 25.6 g of 4,4-diacetyl-5-(ethoxycarbonyl)-heptanedioic acid diethyl ester (boiling point: 170° C./0.002 mbar; purity: 93%; colorless). Content of the active structural element C3O2: 18%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166648B2
Source datasetuspto-grants-2007_01
ORD IDord-43fcb3f4a3f94e9d8d73a58231cdb343
Source noteuspto-grants-2007_01