HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957098Generated: November 2, 2026
Phenethyl bromide → 1,3-Diethyl 2-(2-phenylethyl)propanedioate
https://huagongshe.com/reaction/1957098
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Diethyl 2-(2-phenylethyl)propanedioate | HCID 81119 | 76.6% |
Reaction Steps
123.4 g of potassium tert-butoxide were added in portions, at a temperature of 15° C., to a solution of 160.1 g of diethyl malonate in one litre of dimethylformamide. The reaction mixture was stirred for 30 minutes and a solution of 207.7 g of phenethyl bromide in 200 ml of dimethylformamide was then added dropwise at room temperature. The reaction mixture was subsequently heated at 60° C. for one hour and then allowed to cool down once again. The dimethylformamide was evaporated off under reduced pressure and the remaining residue was taken up in a mixture of methyl tert-butyl ether and water. The organic phase was separated, washed with water, dried over sodium sulfate and evaporated. The crude product, which remained as an oily residue, was purified by distillation under reduced pressure. 202.5 g of ethyl 2-ethoxycarbonyl-4-phenylbutanoate were obtained, b.p.1.5 =148°-153° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05783573 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-f315c58361c9445ab2ad7f279caf5f02 |
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| Source note | uspto-grants-1998_07 |
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