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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493035Generated: October 26, 2026

Hydrochloric Acid → (4-Propylphenyl)methanol

https://huagongshe.com/reaction/493035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 4-propylbenzoateHCID 12861010—
ReactantAluminium lithium hydrideHCID 21226445—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(4-Propylphenyl)methanolHCID 276047298.5%

Reaction Steps

Dried tetrahydrofuran (50 ml) in which 10.4 g (58.4 mmol) of 4-n-propylbenzoic acid methyl ester synthesized in step (i) was dissolved was dropwise added to 50 ml of dried tetrahydrofuran containing suspension of lithium aluminium hydride (1.54 g: 40.5 mmol) at a temperature of not more than 10° C. with cooling with ice, and reaction was carried out at a room temperature overnight. After the completion of the reaction, an excess amount of lithium aluminium hydride was reacted with methanol with cooling with ice. Next water and an aqueous solution of hydrochloric acid were successively added to the reaction mixture, and the resultant was extracted with hexane. After the hexane phase was washed with water, hexane was removed from the hexane phase to give 8.63 g (57.5 mmol) of 4-n-propylbenzyl alcohol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534547B2
Source datasetuspto-grants-2009_05
ORD IDord-a6779d30ec104bc38523bca87f1e820f
Source noteuspto-grants-2009_05