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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103648Generated: October 29, 2026

Tetrahydrofuran → (E)-Ethyl 3-cyclohexylacrylate

https://huagongshe.com/reaction/2103648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCyclohexanecarboxaldehydeHCID 16275—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178477249HCID 178477249—
SolventHexaneHCID 8058—
Product(E)-Ethyl 3-cyclohexylacrylateHCID 5358357—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576108B2
Source datasetuspto-grants-2009_08
ORD IDord-b90066380cb94604bad88b4cf3df3718
Source noteuspto-grants-2009_08