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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768120Generated: November 3, 2026

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

https://huagongshe.com/reaction/1768120

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 aluminum 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 numberUS07235570B2
Source datasetuspto-grants-2007_06
ORD IDord-14017087944640269ad5bb83b0607ca8
Source noteuspto-grants-2007_06