HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → Diethyl 4-[14-(trimethylsilyl)tetradecylamino]benzoylmalonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[14-(Trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride | HCID 20198230 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Diethyl 4-[14-(trimethylsilyl)tetradecylamino]benzoylmalonate | HCID 20198253 | — |
Reaction Steps
A solution of 26.6 g. of diethyl malonate and 10 ml. of 1,2-dimethoxyethane is added to a suspension of 4.0 g. of sodium hydride in 1,2-dimethoxyethane under argon. A solution of 16.9 g. of 4-[14-(trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride in 1,2-dimethoxyethane is then added. The reaction mixture is refluxed for 4.5 hours, cooled, poured on ice, acidified, and extracted with ether. The ether solution is washed with water and saturated sodium chloride solution, dried with anhydrous sodium sulfate and evaporated to dryness. Addition of a small amount of ethanol to the residue gives a solid which is filtered and discarded. The ethanol filtrate is evaporated and the residue is recrystallized to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670421 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-ae6f7d9d6bdc4bbc9260b5b9a582def7 |
| Source note | uspto-grants-1987_06 |