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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061734Generated: November 3, 2026

Sulfuric Acid → 3'-Hydroxybiphenyl-2-carbonitrile

https://huagongshe.com/reaction/1061734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3'-Amino-biphenyl-2-carbonitrileHCID 1393112—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3'-Hydroxybiphenyl-2-carbonitrileHCID 1143551065%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3′-aminobiphenyl-2-carbonitrile (10.9 g, 56 mmol) in 1,4-dioxane (30 ml) was treated with a solution of 25% aqueous sulfuric acid (150 ml). The resulting suspension was cooled to 0° C. before being treated dropwise over 10 minutes with a solution of sodium nitrite (4.6 g, 67 mmol) in water (10 ml). After stirring at 0° C. for 30 minutes the reaction was poured into hot (70° C.) water (500 ml). On cooling to ambient temperature the product was extracted into ethyl acetate (500 ml), the organics were washed with water (300 ml), brine (300 ml) and dried over anhydrous sodium sulfate. Filtration and concentration in vacuo afforded 3′-hydroxybiphenyl-2-carbonitrile as a dark oil (7.1 g, 65%): δH (400 MHz, CDCl3) 5.40 (1H, br), 6.92 (1H, ddd, J 8, 3 and 1), 7.04 (1H, dd, J 3 and 3), 7.11 (1H, ddd, J 8, 3 and 1), 7.35 (1H, dd, J 8 and 8), 7.44 (1H, ddd, J 8, 8 and 1), 7.51 (1H, dd, J 8 and 1), 7.64 (1H, ddd, J 8, 8 and 1), 7.75 (1H, dd, J 8 and 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06960598B2
Source datasetuspto-grants-2005_11
ORD IDord-904062750d6f4dca8df269f87b5b9081
Source noteuspto-grants-2005_11