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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424853Generated: October 30, 2026

Hydrochloric Acid → 2-Ethoxy-6-pentadecyl-benzyl alcohol

https://huagongshe.com/reaction/424853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl AcetateHCID 8857—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantEthyl 2-Ethoxy-6-pentadecylbenzoateHCID 22574569—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexaneHCID 21226206—
Product2-Ethoxy-6-pentadecyl-benzyl alcoholHCID 66701924—

Reaction Steps

Ethyl 2-ethoxy-6-pentadecyl-benzoate (10.9 g, 27 mmol) was dissolved in dry tetrahydrofuran (60 mL). This solution was transferred to dry 250 mL three neck round bottom flask fitted with reflux condenser, mechanical stirrer and it was maintained under nitrogen atmosphere through out the reaction. To this lithium aluminum hydride (2.04 g, 54 mmol) was added slowly. Reaction was highly exothermic. After addition the solution was slowly brought to the reflux temperature and maintained at that temperature for about two hours and TLC was checked in hexane:EtOAc (8:2). After completion of reaction, excess lithium aluminium hydride was decomposed by drop-wise addition of ethylacetate (80 mL). To this 5 M HCl (100 mL) was added and organic layer was separated, dried over anhydrous sodium sulphate, concentrated under vacuum to give a light brownish solid. This was recrystallised from petroleum ether (40-60° C.) to give white solid. Yield: 8 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106062B1
Source datasetuspto-grants-2012_01
ORD IDord-5eda61ffb7e040c49c913b22ac80eb06
Source noteuspto-grants-2012_01