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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390211Generated: October 27, 2026

Benzenesulfonyl chloride → HCID 58625075, compound

https://huagongshe.com/reaction/390211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant3-(3-Dimethoxymethyl-4-nitro-phenoxy)phenylamineHCID 58625052—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58625075HCID 58625075—

Reaction Steps

A mixture of 3-(3-dimethoxymethyl-4-nitro-phenoxy)phenylamine (0.013 mol) in THF (100 mL) and TEA (200 mL) was stirred at room temperature and a mixture of benzenesulfonyl chloride (0.013 mol) in THF (50 mL) was added dropwise, then the reaction mixture was stirred overnight at room temperature and again overnight at 60° C. The solvent was evaporated and the residue was stirred in H2O. After extraction with CH2Cl2, the organic layer was separated, dried, filtered off and the solvent was evaporated. The residue was purified by Biotage column chromatography (eluent: CH2Cl2 100%). The purest product fractions were collected and the solvent was evaporated to yield the title compound as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383637B2
Source datasetuspto-grants-2013_02
ORD IDord-329c5565965e435f9042e6e8d104e8aa
Source noteuspto-grants-2013_02