HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22928Generated: October 25, 2026
Hydrochloric Acid → 2-Hydroxy-4-methylbenzaldehyde
https://huagongshe.com/reaction/22928
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | M-Cresol | HCID 342 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Hydroxy-4-methylbenzaldehyde | HCID 61200 | 25.5% |
Reaction Steps
To a stirred solution of 3-methyl-phenol (1 g, 9.2 mmol) in toluene (5 ml) at room temperature under nitrogen was added SnCl4 (241 mg, 0.92 mmol) and tri-nbutylamine (0.6 ml, 2.77 mmol). After 20 min, paraformaldehyde (611 mg, 20.3 mmol) was added and the whole stirred at 100° C. for 16 h. The reaction mixture was diluted with water (20 ml) and acidified with 2N HCl to pH2. The solution was extracted with ether (25 ml), washed with brine (20 ml), dried (MgSO4) filtered and evaporated to a brown oil. This oil was purified by column chromatography using 5% EtOAc in pentane as eluant to provide the title product (319 mg, 25%); 1HNMR (400 MHz, CDCl3) δ: 2.3 (s, 3H), 6.75 (m, 2H), 7.35 (d, 1H), 9.75 (s, 1H), 11.00 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849649B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-967ddfe73b30491d9915c6116112b85f |
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| Source note | uspto-grants-2005_02 |
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