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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889704Generated: October 31, 2026

3,5-Dichloro-2-hydroxybenzenesulphonyl chloride → HCID 58531699, compound

https://huagongshe.com/reaction/1889704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dichloro-2-hydroxybenzenesulphonyl chlorideHCID 90078—
ReactantHCID 58531372HCID 58531372—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58531699HCID 5853169939%

Reaction Steps

To a solution of 1-(4′-chlorobiphenyl-3-yl)-N-(4-fluorobenzyl)methanamine (70 mg, 0.22 mmol) in THF (4 mL) were added 3,5-dichloro-2-hydroxybenzenesulfonyl chloride (61.8 mg, 0.24 mmol) and TEA (0.08 mL, 0.54 mmol). The resulting mixture was stirred at rt for 1 h and concentrated in vacuo. The residue was dissolved in MeOH and purified by preparative HPLC. Fractions containing the desired product were combined, concentrated, and lyophilized to give the title compound (46 mg, 39%) as a glassy solid. 1H NMR (CD3OD) 7.59 (d, J=4.0 Hz, 1H), 7.43 (d, J=4.0 Hz, 1H), 7.36-7.35 (m, 5H), 7.22 (t, J=8.0 Hz, 1H), 7.16-7.09 (m, 5H), 7.05-7.03 (t, J=8.0 Hz, 1H), 6.90-6.85 (m, 2H), 4.46 (s, 2H), 4.41 (s, 2H). MS (ESI): 550.0 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-4d523c7f4cbb469eb8f83efd88749722
Source noteuspto-grants-2013_08