HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324248Generated: October 27, 2026
4-Formylbenzoic acid → 4-[3-(8,8-Dimethyl-5-p-tolyl-7,8-dihydro-2-naphthyl)-3-oxopropenyl]benzoic acid
https://huagongshe.com/reaction/324248
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,4-Dihydro-1-(4-methylphenyl)-4,4-dimethyl-6-acetylnaphthalene | HCID 22323776 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-[3-(8,8-Dimethyl-5-p-tolyl-7,8-dihydro-2-naphthyl)-3-oxopropenyl]benzoic acid | HCID 54296652 | — |
Reaction Steps
To a solution of 78.7 mg (0.272 mmol) 3,4-dihydro-1-(4-methylphenyl)-4,4-dimethyl-6-acetylnaphthalene (Compound 100G) in 4.0 ml of MeOH was added 53.1 mg (0.354 mmol) of 4-carboxy benzaldehyde, and 80. mg (2.00 mmol; 2.0 ml of 1M aqueous NaOH). The resulting solution was stirred at room temperature for 12 hours, concentrated under reduced pressure, and the residual oil dissolved in EtOAc. The solution was treated with 10% HCl, and the organic layer was washed with H2O, and saturated aqueous NaCl, then dried over Na2SO4. Removal of the solvents under reduced pressure gave the title compound as a colorless solid which was purified by recrystallization from CH3CN. 1H NMR (acetone-d6): δ 8.00 (7H, m), 7.83 (1H, d, J=15.6 Hz), 7.24 (4H, s), 7.13 (1H, d, J=8.1 Hz), 6.12 (1H, t, J=4.5 Hz), 2.42 (2H, d, J=4.8 Hz), 2.38 (3H, s), 1.41 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218128B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-a2118a7b671d42cabb63088471a4c127 |
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| Source note | uspto-grants-2001_04 |
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