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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906104Generated: October 30, 2026

Dimethylamine → Methyl 4-cyano-3-hydroxybenzoate

https://huagongshe.com/reaction/906104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 4-Bromo-3-hydroxybenzoateHCID 6425184—
Catalystpalladium(II) acetateHCID 167845—
CatalystHCID 178511488HCID 178511488—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-cyano-3-hydroxybenzoateHCID 1664112933.5%

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012956B2
Source datasetuspto-grants-2011_09
ORD IDord-bbd9fe90828143d39757e911b1e99f73
Source noteuspto-grants-2011_09