Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626237Generated: October 30, 2026

[4-(2-Chloroethoxy)phenyl](4-hydroxyphenyl)methanone → 4-(2-(Benzo[c][1,2,5]thiadiazol-5-yl)-1-(4-(2-chloro-ethoxy)phenyl)but-1-enyl)phenol

https://huagongshe.com/reaction/626237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[4-(2-Chloroethoxy)phenyl](4-hydroxyphenyl)methanoneHCID 89656364—
Reactant1-(Benzo[c][1,2,5]thiadiazol-5-yl)propan-1-oneHCID 89657553—
Product4-(2-(Benzo[c][1,2,5]thiadiazol-5-yl)-1-(4-(2-chloro-ethoxy)phenyl)but-1-enyl)phenolHCID 13650289910%

Reaction Steps

According to general procedure of McMurry reaction as example 1, step D described, 1-(benzo[c][1,2,5]thiadiazol-5-yl)propan-1-one (552 mg, 2 mmol) was reacted with (4-(2-chloroethoxy)phenyl)(4-hydroxyphenyl)methanone (384 mg, 2 mmol) to give the desired product (83 mg, 10%, Z/E=1/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309211B2
Source datasetuspto-grants-2016_04
ORD IDord-b3c130df9c824efca71603cc5a4148c8
Source noteuspto-grants-2016_04