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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249417Generated: November 3, 2026

1-Chloro-4-(chloromethyl)benzene → 4-carboxy-2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/2249417

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantHCID 23094117HCID 23094117—
Reactant2-(4-fluorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-4-methanesulfonyloxymethyl-2H-pyridazin-3-oneHCID 23094126—
Product4-carboxy-2-(4-chlorobenzyl)-6-(2,3-dihydro-1-benzofuran-5-yl)-2H-pyridazin-3-oneHCID 2309412989.3%

Reaction Steps

The general procedure of Example 1 (3) was carried out by use of 6-(2,3-dihydro-1-benzofuran-5-yl)-4-methoxycarbonyl-2H-pyridazin-3-one and 4-chlorobenzyl chloride, to thereby yield the title compound as a yellow powder (yield: 89.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314877B2
Source datasetuspto-grants-2008_01
ORD IDord-302deba9708b45eb859dbd7cd64f99cc
Source noteuspto-grants-2008_01