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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7691Generated: October 26, 2026

Water → 5'-(1,3-Benzoxazol-2-yl)-2'-(cyanomethyl)-1,1'-biphenyl-3-carbonitrile

https://huagongshe.com/reaction/7691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant5'-(1,3-Benzoxazol-2-yl)-2'-(bromomethyl)-1,1'-biphenyl-3-carbonitrileHCID 21990971—
SolventDimethylformamideHCID 6228—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product5'-(1,3-Benzoxazol-2-yl)-2'-(cyanomethyl)-1,1'-biphenyl-3-carbonitrileHCID 10193442—

Reaction Steps

A mixture of 5′-(1,3-benzoxazol-2-yl)-2′-(bromomethyl)-1,1′-biphenyl-3-carbonitrile (183 mg, 0.47 mmol) and sodium cyanide (46 mg, 0.94 mmol) in DMF:H2O (5:1, 18 mL) and DMF (20 mL) was stirred at rt for 3 h. H2O was added to the reaction mixture and it was extracted with EtOAc (3×). The organics were combined, washed with brine (2×), dried over Na2SO4, and evaporated to dryness to give an orange oil. The crude was purified by flash chromatography on silica gel eluting with a gradient of EtOAc:hexanes (0 to 30 min: 0 to 20% EtOAc) to afford the desired 5′-(1,3-benzoxazol-2-yl)-2′-(cyanomethyl)-1,1′-biphenyl-3-carbonitrile as a colorless solid (M.p. 175–176° C.). 1H NMR (CDCl3, 300 MHz) δ 8.34 (dd, 1H), 8.18 (s, 1H), 7.77 (m, 3H), 7.67 (m, 3H), 7.60 (m, 1H), 7.40 (m, 2H), 3.69 (s, 2H). MS (ESI) 336 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087601B2
Source datasetuspto-grants-2006_08
ORD IDord-6ff639e34c174f3f9b057cc7f2257246
Source noteuspto-grants-2006_08