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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789556Generated: October 30, 2026

Ethyl 5-ethoxyheptanoate → 5-Ethoxyheptanol

https://huagongshe.com/reaction/1789556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-ethoxyheptanoateHCID 13924080—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product5-EthoxyheptanolHCID 15053038—

Reaction Steps

A solution of tetrahydrofuran (2000 ml) and lithium aluminum hydride (46 g, 1.21 moles) is cooled in a -60° C. dry ice/ethanol bath. The starting material prepared in Example 36, ethyl 5-ethoxyheptanoate (302 g ,1.49 moles) is diluted in tetrahydrofuran (300 ml) and added dropwise to the stirring reaction. After the addition is complete the reaction is warmed to room temperature and stirred for an additional hour. The solution is cooled in a -78° C. dry ice/ethanol bath and the excess hydride is destroyed by adding dropwise the following: water (46 ml), 15% sodium hydroxide solution (46 ml), and water (136 ml). The reaction is filtered and the solids washed several times with tetrahydrofuran (3×500 ml). The volume of the filtrate is reduced under vacuum and the residue dried over anhydrous magnesium sulfate. The remaining solvent is then removed leaving a clear, colorless oil suitably pure for the next reaction (238 g, 1.49 moles).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04689345
Source datasetuspto-grants-1987_08
ORD IDord-9304ce1b45c546198b92a8d99296d05b
Source noteuspto-grants-1987_08