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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1598835Generated: October 31, 2026

4-Chlorophenylboronic acid → HCID 10641092, compound

https://huagongshe.com/reaction/1598835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantHCID 10710131HCID 10710131—
ProductHCID 10641092HCID 1064109274.9%

Reaction Steps

Following the general procedure outlined in Synthetic Scheme VI, 2.3 g (7.4 mmol) of 1-bromo-2-[4-(methylsulfonyl)phenyl]benzene (Example 4, Step 2) was reacted with 1.7 g (11 mmol) of 4-chlorophenylboronic acid. Purification by silica gel chromatography (Waters Prep-500A) with ethyl acetate/hexane (1:3) and subsequent recrystallization from ethyl acetate/hexane gave 1.90 g (74%) of 1-(4-chlorophenyl)-2-[4-(methylsulfonyl)phenyl]benzene as a colorless solid: mp 180.2°-180.6° C.; NMR (CDCl3) δ 3.06 (s, 3H), 7.04 (d, J=8 Hz, 2H), 7.21 (d, J=8 Hz, 2H), 7.33 (d, J=9 Hz, 2H), 7.38-7.51 (m, 4H), 7.81 (d, J=8 Hz, 2H). MS (EI): m/e (rel intensity) 342 (34), 228 (100); HRMS Calc'd for C19H15ClO2S: 342.0481. Found: 342.0484. Anal. Calc'd for C19H15ClO2S: C, 66.56; H, 4.41; Cl, 10.34. Found: C, 66.45; H, 4.48; Cl, 10.63.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05739166
Source datasetuspto-grants-1998_04
ORD IDord-215ddc7f21ad4edcad6e608e74c4c797
Source noteuspto-grants-1998_04