HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 4,4-Diacetyl-5-(ethoxycarbonyl)-heptanedioic acid diethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Diethyl fumarate | HCID 638144 | — |
| Reactant | Hexanoic acid, 4-acetyl-5-oxo-, ethyl ester | HCID 2733934 | — |
| Catalyst | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4,4-Diacetyl-5-(ethoxycarbonyl)-heptanedioic acid diethyl ester | HCID 58784953 | 53.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166648B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-43fcb3f4a3f94e9d8d73a58231cdb343 |
| Source note | uspto-grants-2007_01 |