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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598828Generated: October 31, 2026

4-Bromobenzenesulfonamide → HCID 10782440, compound

https://huagongshe.com/reaction/1598828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
ReactantHCID 22610240HCID 22610240—
ProductHCID 10782440HCID 1078244046%

Reaction Steps

Following the general procedure outlined in Synthetic Scheme IX, 1.5 g (6.9 mmol) of 2-(4-fluorophenyl)phenylboronic acid (Step 1) was reacted with 2.5 g (10.4 mmol) of 4-bromobenzenesulfonamide (Lancaster). Purification by silica gel chromatography (Waters LC-2000) with ethyl acetate/hexane (3:7) and subsequent recrystallization from ethyl acetate/hexane gave 1.04 g (46%) of 4-[2-(4-fluorophenyl)phenyl] benzenesulfonamide as a colorless solid: mp 187.3--188.2° C.; NMR (CDCl3) δ 4.83 (s, 2H), 6.92 (t, J=9 Hz, 2H), 7.02-7.11 (m, 2H), 7.27 (d, J=9 Hz, 2H), 7.36-7.50 (m, 4H), 7.78 (d, J=8 Hz, 2H). MS (EI): m/e (rel intensity) 327 (75) 245 (100); HRMS Calc'd for C18H14FNO2S: 327.0729. Found: 327.0743. Anal. Calc'd for C18H14FNO2S: C, 66.04; H, 4.31; N, 4.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739166
Source datasetuspto-grants-1998_04
ORD IDord-6b84a2e0330946dea1f6a921799cc254
Source noteuspto-grants-1998_04