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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900519Generated: October 30, 2026

Hydrochloric Acid → 2-(3-Hydroxy-1-phenylpropyl)-4-methylphenol

https://huagongshe.com/reaction/900519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant6-Methyl-4-phenyl-3,4-dihydrochromen-2-oneHCID 3791643—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventAcetone cyclohexaneHCID 21916603—
Product2-(3-Hydroxy-1-phenylpropyl)-4-methylphenolHCID 1148190586%

Reaction Steps

A basic aqueous solution of sodium borohydride prepared beforehand by dissolving 23.8 g (0.630 moles) of NaBH4 at ambient temperature in 170 ml of H2O and 3.5 ml of 30% wt./vol. NaOH was added dropwise to a suspension of 3,4-dihydro-6-methyl-4-phenyl-2H-benzopyran-2-one of the formula (II) (100 g, 0.420 moles) in isopropanol (200 ml). Once addition was complete, the temperature was adjusted to 60° C. and the course of the reaction was monitored by TLC (eluent: cyclohexane/acetone: 70/30) until the substrate had completely disappeared. After 5 h, the reaction mixture was cooled to ambient temperature and HCl (2N) was added until a final pH of 7.0 was obtained. Stirring was continued for 30 min at ambient temperature, then the resultant suspension was filtered through a Buchner filter. The filtered solution was concentrated under reduced pressure and the crude residue was crystallised from toluene (280 ml) to yield 87.4 g (yield 86%) of 3-(2-hydroxy-5-methylphenyl)-3-phenylpropanol (VIII) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358399B2
Source datasetuspto-grants-2008_04
ORD IDord-738e111c0df74c1dbf486ff147ca4876
Source noteuspto-grants-2008_04