Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7684Generated: October 26, 2026

Water → [4-(1,3-Benzoxazol-2-yl)-2-bromophenyl]acetonitrile

https://huagongshe.com/reaction/7684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CyanideHCID 8929—
Reactant2-[3-Bromo-4-(bromomethyl)phenyl]-1,3-benzoxazoleHCID 21990988—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
Product[4-(1,3-Benzoxazol-2-yl)-2-bromophenyl]acetonitrileHCID 10236618—

Reaction Steps

A mixture of 2-[3-bromo-4-(bromomethyl)phenyl]-1,3-benzoxazole (156 mg, 0.42 mmol), and sodium cyanide (41 mg, 0.84 mmol) in DMF:H2O (3:1, 16 mL) was stirred at rt for 18 h. Water (50 mL) 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 oil was purified by flash chromatography eluting with a gradient of EtOAc:hexane (0 to 30 min: 0 to 20% EtOAc) to afford the desired [4-(1,3-benzoxazol-2-yl)-2-bromophenyl]acetonitrile as a yellow solid (M.p. 190–191° C.). 1H NMR (CDCl3, 300 MHz) δ 8.50 (s, 1H), 8.22 (dd, 1H), 7.78 (m, 1H), 7.70 (d, 1H), 7.60 (m, 1H), 7.39 (m, 2H), 3.91 (s, 2H). MS (ESI) 313 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087601B2
Source datasetuspto-grants-2006_08
ORD IDord-523f9f484d514ad4a74e2e1e4162434e
Source noteuspto-grants-2006_08