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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597769Generated: October 26, 2026

Sulfuric Acid → (4-Propylphenyl)methanol

https://huagongshe.com/reaction/597769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant4-Propylbenzoic acidHCID 137601—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product(4-Propylphenyl)methanolHCID 276047290.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of sodium borohydride (2.9 g, 76 mmol) and concentrated sulfuric acid in ether (prepared by adding 2.0 ml of concentrated sulfuric acid to 4.0 ml of ether) was added dropwise to a solution of p-n-propylbenzoic acid (5.0 g, 32 mmol) in tetrahydrofuran (20 ml) cooled to 0° C. keeping the temperature of the reaction system below 20° C., and then this mixture was stirred at room temperature for 3 hours. After the mixture was cooled on ice, methanol and 1 N sodium hydroxide were added, and this mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to give the title compound (4.33 g). This compound was used in the following reaction without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897387B2
Source datasetuspto-grants-2011_03
ORD IDord-d0dd117975bb4f1fa1b0064a511fcf44
Source noteuspto-grants-2011_03