HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl cyanoacetate → HCID 13632645, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl cyanoacetate | HCID 7747 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18860-95-2 | HCID 205858 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13632645 | HCID 13632645 | 102.3% |
Reaction Steps
A mixture of 65.3 g of methyl cyanoacetate, 228 g of freshly pulverized potassium carbonate and 800 ml of anhydrous tetrahydrofuran was heated at reflux under nitrogen for 2 hours. A solution of 150.5 g of 1,4-dibromo-2-methyl-2-butene in 500 ml of anhydrous tetrahydrofuran was added slowly dropwise to the refluxing reaction mixture over a period of two days. The solids were removed from the cooled reaction mixture by filtration through a bed of celite. The filtrate was concentrated in vacuo to leave 111.4 g of yellow oil. Distillation of the oil gave 81.3 g of the desired product as a colorless oil: b.p. 95°-105° C. (0.05 mm Hg) consisting of two isomers in a ratio of 2:1 by GLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04588821 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-ea186d174e804d59ae6240a0c212c3c5 |
| Source note | uspto-grants-1986_05 |