HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103648Generated: October 29, 2026
Tetrahydrofuran → (E)-Ethyl 3-cyclohexylacrylate
https://huagongshe.com/reaction/2103648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexanecarboxaldehyde | HCID 16275 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178477249 | HCID 178477249 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (E)-Ethyl 3-cyclohexylacrylate | HCID 5358357 | — |
Reaction Steps
Add triethylphospinoacetate (185 g, 821 mmol) to a suspension of hexane-washed sodium hydride (34.5 g, 60%, 862 mmol) in THF (1 L) at 0° C. Stir the resulting mixture for 1 h, and then cool it to −78° C. Then add a solution of cyclohexylmethanal (92.2 g, 821 mmol) in THF (500 mL) dropwise over 90 min, maintaining an internal temperature of less than −68° C. Allow the reaction mixture to warm to r.t. over 18 h. Then add a solution of saturated aqueous ammonium chloride solution (1 L) to the reaction mixture carefully. Extract the resulting mixture with ether (3×1 L). Combine the extracts and wash them with water (2×1 L), followed by saturated aqueous sodium chloride solution (1 L). Then dry the extracts over magnesium sulfate, and concentrate the solution under vacuum to afford the title compound as a yellow oil (154.8 g). GC-MS (m/e): 182 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07576108B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b90066380cb94604bad88b4cf3df3718 |
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| Source note | uspto-grants-2009_08 |
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