HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906104Generated: October 30, 2026
Dimethylamine → Methyl 4-cyano-3-hydroxybenzoate
https://huagongshe.com/reaction/906104
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 4-Bromo-3-hydroxybenzoate | HCID 6425184 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | HCID 178511488 | HCID 178511488 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-cyano-3-hydroxybenzoate | HCID 16641129 | 33.5% |
Reaction Steps
To a solution of methyl 4-bromo-3-hydroxybenzoate (1.01 g, 4.4 mmol) in 7 ml of dimethylamine was added Pd(OAc)2 (15 mg, 0.5 mol %), sodium carbonate (0.47 g, 4.4 mmol) and potassium ferricyanide (0.41 g, 0.97 mmol). The mixture was heated to 120° C. and stirred at this temperature for 4 hours and at RT for 18 hours. The reaction mixture was diluted with 30 ml of ethyl acetate and the resulting slurry was filtered through Celite. The filtrate was washed with water (2×15 ml) and 5% aqueous ammonium hydroxide (1×15 ml). The organic layer was dried over sodium sulfate, filtered and concentrated to provide methyl 4-cyano-3-hydroxybenzoate (0.26 g, 33.5% yield) (S. Weissman, D. Zewge, C. Chen; J. Org. Chem. 2005, 70, 1508-1510). 1H NMR (400 MHz, CD3OD): 7.65 (d, 1H), 7.56-7.54 (m, 2H), 3.91 (s, 3H). MS (EI) for C9H7NO3: 178 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012956B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-bbd9fe90828143d39757e911b1e99f73 |
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| Source note | uspto-grants-2011_09 |
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