HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117232Generated: October 27, 2026
Potassium Carbonate → 2-(2-Formyl-6-methylphenoxy)acetonitrile
https://huagongshe.com/reaction/2117232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 3-Methylsalicylaldehyde | HCID 522777 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Formyl-6-methylphenoxy)acetonitrile | HCID 22241345 | — |
Reaction Steps
A mixture of 2-hydroxy-3-methylbenzaldehyde (10.2 g, 75.0 moles, Aldrich), bromoacetonitrile (5.70 mL, 82.5 mmoles), and potassium carbonate (11.4 g, 82.5 mmoles) in DMF (150 mL) is heated to 55° C. for 3 hours, cooled, then diluted with ether. The mixture is washed with distilled water, saturated NaCl solution, then the organic layer dried over MgSO4 and concentrated to give the title compound as a yellow solid. 1H NMR (300 MHz, CDCl3): δ 10.20 (s, 1H), 7.70 (d, 1H), 7.53 (d, 1H), 7.29 (m, 1H), 4.81 (s, 2H), 2.42 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE040558E1 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-ce742649d16d40d9b48008dcd626b4d4 |
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| Source note | uspto-grants-2008_10 |
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