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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645031Generated: October 25, 2026

3,4-Dichlorophenol → 3-(4,5-dichloro-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/645031

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorophenolHCID 7258—
ReactantSesamolHCID 68289—
Reactant1-Pentyl-1H-indole-2,3-dioneHCID 1581092—
Reactant4-bromo-1-pentyl-1H-indole-2,3-dioneHCID 28492458—
Product3-(4,5-dichloro-2-hydroxyphenyl)-3-hydroxy-1-pentyl-1,3-dihydro-2H-indol-2-oneHCID 58872503—

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 3,4-dichlorophenol, the title compound was obtained (26%): 1H NMR (300 MHz, CDCl3) δ 9.60 (s, 1H), 7.50-7.40 (m, 2H), 7.22 (td, 1H), 7.11 (s, 1H), 6.95 (d, 1H), 6.86 (s, 1H), 4.31-4.12 (br, 1H), 3.79-3.59 (m, 2H), 1.76-1.62 (m, 2H), 1.40-1.27 (m, 4H), 0.88 (t, 3H); MS (ES+) m/z 363 (M−17), 403 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700641B2
Source datasetuspto-grants-2010_04
ORD IDord-b4713ebb613e474ea098535a99b674db
Source noteuspto-grants-2010_04