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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-Methyl-4-phenyl-3,4-dihydrochromen-2-one | HCID 3791643 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Acetone cyclohexane | HCID 21916603 | — |
| Product | 2-(3-Hydroxy-1-phenylpropyl)-4-methylphenol | HCID 11481905 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358399B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-738e111c0df74c1dbf486ff147ca4876 |
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| Source note | uspto-grants-2008_04 |
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