Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1806772Generated: October 31, 2026

Benzeneacetonitrile, 4-bromo- → HCID 59249234, compound

https://huagongshe.com/reaction/1806772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneacetonitrile, 4-bromo-HCID 27914—
Reactant3-Chloro-2-fluorobenzaldehydeHCID 736335—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 59249234HCID 59249234100.8%

Reaction Steps

In a manner similar to the method described in Example 1b, 4-bromophenylacetonitrile (Aldrich) (4.5 g, 23 mmol) was reacted with 3-chloro-2-fluorobenzaldehyde (5.2 g, 33 mmol), methanolic solution (25 wt %) of sodium methoxide (15 mL, 66 mmol) in methanol (150 mL) at 50° C. for 3 h to give (Z)-2-(4-bromo-phenyl)-3-(3-chloro-2-fluoro-phenyl)-acrylonitrile as a white powder (7.8 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354444B2
Source datasetuspto-grants-2013_01
ORD IDord-5155e53fd60a4570be90c0d7e3862676
Source noteuspto-grants-2013_01