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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839942Generated: October 27, 2026

(2H-1,3-benzodioxol-5-yl)boronic acid → 5-[4,5-Difluoro-2-[4-(methylsulfonyl)phenyl]phenyl]-1,3-benzodioxole

https://huagongshe.com/reaction/1839942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2H-1,3-benzodioxol-5-yl)boronic acidHCID 2734371—
Reactant1-Bromo-4,5-difluoro-2-[4-(methylsulfonyl)phenyl]benzeneHCID 11791923—
Product5-[4,5-Difluoro-2-[4-(methylsulfonyl)phenyl]phenyl]-1,3-benzodioxoleHCID 1050046699%

Reaction Steps

Following the general procedure outlined in Synthetic Scheme I, 2.24 g (6.45 mmol) of 1-bromo-4,5-difluoro-2-[4-(methylsulfonyl)phenyl]benzene (Example 18, Step 2) was reacted with 1.39 g (8.38 mmol) of (1,3-benzodioxol-5-yl)boronic acid (Step 1). Purification by silica gel chromatography (MPLC) with ethyl acetate/hexane (1:4) gave 2.47 g (99%) of 5-[4,5-difluoro-2-[4-(methylsulfonyl)phenyl]phenyl]-1,3-benzodioxole as a colorless solid: mp 110.0-111.0° C.; NMR (CDCl3) δ 3.05 (s, 3H), 5.95 (s, 2H), 6.47-6.52 (m, 2H), 6.67 (d, J=8.5 Hz, 1H),-7.16-7.24 (m, 2H), 7.32 (d, J=8.5 Hz, 2H), 7.82 (d, J=8.5 Hz, 2H). MS (FAB): m/e 395 (M+Li). Anal. Calc'd for C20H14F2O4S: C, 61.85; H, 3.63. Found: C, 61.92; H, 3.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677488B2
Source datasetuspto-grants-2004_01
ORD IDord-0a0f7e311a82498e8739c2b3b006c58f
Source noteuspto-grants-2004_01