HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16647Generated: October 26, 2026
Sodium Chloride → Ethyl (2E)-3-phenyl-2-butenoate
https://huagongshe.com/reaction/16647
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (2E)-3-phenyl-2-butenoate | HCID 5354836 | 128.9% |
Reaction Steps
A mixture of 10 g (0.25 mol) of sodium hydride and tetrahydrofuran is heated to 50° C., followed by dropwise addition over 30 minutes of a solution of 48 ml (0.19 mol) of ethyl diethylphosphonoacetate in 80 ml of tetrahydrofuran. A solution of 28.4 g (0.24 mol) of acetophenone in 60 ml of tetrahydrofuran is added dropwise at 0° C. and the mixture is stirred for 16 hours at 25° C. 250 ml of saturated sodium chloride solution are added at 0° C. and the resulting mixture is extracted with ether. The organic phase is dried (Na2SO4) and the solvents are evaporated off under reduced pressure. The 46.6 g of product obtained are purified by flash chromatography (90/10 cyclohexane/diisopropyl ether) (29 g; 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737176B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-e57508df4c494718b30ab937cbf2203a |
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| Source note | uspto-grants-2010_06 |
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