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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425558Generated: October 26, 2026

Sesamol → ethyl [5-chloro-3-hydroxy-3-(6-hydroxy-2,3-dihydro-1-benzofuran-5-yl)-2-oxo-2,3-dihydro-1H-indol-1-yl]acetate

https://huagongshe.com/reaction/425558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSesamolHCID 68289—
Reactant2,3-Dihydro-1-benzofuran-6-olHCID 12236540—
Reactant4-bromo-1-pentyl-1H-indole-2,3-dioneHCID 28492458—
ReactantEthyl 2-(5-chloro-2,3-dioxoindolin-1-yl)acetateHCID 28492634—
Productethyl [5-chloro-3-hydroxy-3-(6-hydroxy-2,3-dihydro-1-benzofuran-5-yl)-2-oxo-2,3-dihydro-1H-indol-1-yl]acetateHCID 58872441—

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 ethyl (5-chloro-2,3-dioxo-2,3-dihydro-1H-indol-1-yl)acetate, and 1,3-benzodioxol-5-ol with 2,3-dihydrobenzofuran-6-ol, the title compound was obtained (85%) as a white solid: 1H NMR (300 MHz, CDCl3) δ 8.70 (br, 1H), 7.31-7.24 (m, 2H), 6.92 (d, 1H), 6.68 (s, 1H), 6.46 (s, 1H), 4.53-4.46 (m, 2H), 5.09-4.40 (d, 2H), 4.18 (q, 2H), 3.08-2.88 (m, 2H), 1.23 (t, 3H); MS (ES+) m/z 387.8 (M−17).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106087B2
Source datasetuspto-grants-2012_01
ORD IDord-002828b91bff4ffb9e193cc8daf58c98
Source noteuspto-grants-2012_01