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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545783Generated: October 29, 2026

3-Bromophenol → 3-(4-bromo-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/545783

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
ReactantSesamolHCID 68289—
Reactant1-Pentyl-1H-indole-2,3-dioneHCID 1581092—
Reactant4-bromo-1-pentyl-1H-indole-2,3-dioneHCID 28492458—
Product3-(4-bromo-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-oneHCID 58872516—

Reaction Steps

Following the procedure as described in PREPARATION 1C, and making non-critical variations to replace 4-bromo-1-pentyl-1H-indole-2,3-dione with 1-pentyl-1H-indole-2,3-dione, and 1,3-benzodioxol-5-ol with 3-bromophenol, the title compound was obtained (48%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 9.66 (br, 1H), 7.50-7.38 (m, 2H), 7.24-7.16 (m, 2H), 6.98-6.86 (m, 2H), 6.64 (d, 1H), 4.15 (br, 1H), 3.80-3.55 (m, 2H), 1.75-1.62 (m, 2H), 1.40-1.34 (m, 4H), 0.89 (t, 3H); MS (ES+) m/z 391.4 (M+1), 393.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935721B2
Source datasetuspto-grants-2011_05
ORD IDord-4b2754b6a08e4a91b4434bf1dd2e59f5
Source noteuspto-grants-2011_05