HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361295Generated: October 31, 2026
1,2,3-Trimethylbenzene → 2,3,4-trimethylbenzaldehyde
https://huagongshe.com/reaction/361295
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2,3-Trimethylbenzene | HCID 10686 | — |
| Reactant | Methane, dichloromethoxy- | HCID 21004 | — |
| Reactant | Tin tetrachloride | HCID 24287 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3,4-trimethylbenzaldehyde | HCID 2752597 | — |
Reaction Steps
To a stirred solution of SnCl4 (39 g, 0.15 mol) in 50 mL of dichloromethane was added dropwise at -5° C. a solution of 15 g (0.13 mol) of dichloromethylmethylether. This solution was stirred at -5° C. for one hour before adding dropwise over 10 min a solution of 12 g (0.1 mol) of 1,2,3-trimethylbenzene. The mixture was stirred at 0° C. for 15 min before warming to room temperature where it was stirred an additional 1.5 hrs. After quenching onto 100 g of ice the organic layer was separated, washed with water, saturated aqueous sodium bicarbonate and water before drying over Na2SO4, filtering and evaporating to dryness in vacuo. The product was purified by distillation in vacuo. B.p. 120°-122° C. (11 mm). Lit. b.p. 121.5 (11 mm) Yield: 9.2 g (70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866513 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-33a27399976e435da7c4122130599136 |
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| Source note | uspto-grants-1999_02 |
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