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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071787Generated: October 25, 2026

1-Chloro-4-iodobenzene → 4-Acetyl-4'-chloro-2-nitrobiphenyl

https://huagongshe.com/reaction/2071787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-iodobenzeneHCID 12510—
Reactant1-(4-Bromo-3-nitrophenyl)ethan-1-oneHCID 87737—
SolventMethanolHCID 887—
Product4-Acetyl-4'-chloro-2-nitrobiphenylHCID 21320563—

Reaction Steps

4-Chloroiodobenzene and 4-bromo-3-nitroacetophenone were reacted under Ullmann conditions to give the novel intermediate 4-acetyl-4'-chloro-2-nitrobiphenyl, m.p. 103°-105° C. (from methanol). This compound was reduced with stannous chloride and concentrated hydrochloric acid to give 4-acetyl-2-amino-4'-chlorobiphenyl, m.p. 139°-140° C. (from methanol).This compound was converted to the novel intermediate 4-acetyl-4'-chloro-2-hydroxybiphenyl and thence to the novel intermediate 4-acetyl-4'-chloro-2-methoxybiphenyl, b.p. 167°-170° C./0.4 mm., by diazotization and methylation methods analogous to those described in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04048332
Source datasetuspto-grants-1977_09
ORD IDord-36c8d562051a4322807182b29d42812f
Source noteuspto-grants-1977_09