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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965382Generated: October 31, 2026

3-Bromophenol → 3-(7-chloro-6-hydroxy-2,3-dihydro-1,4-benzodioxin-5-yl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1965382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromophenolHCID 11563—
Reactant1-(diphenylmethyl)-1H-indole-2,3-dioneHCID 1969277—
Reactant1-((5-(Trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dioneHCID 67356488—
Reactant7-Chloro-2,3-dihydrobenzo[b][1,4]dioxin-6-olHCID 67379485—
Product3-(7-chloro-6-hydroxy-2,3-dihydro-1,4-benzodioxin-5-yl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-oneHCID 67356600—

Reaction Steps

Following the procedure as described in PREPARATION 2A and making non-critical variations using 7-chloro-2,3-dihydrobenzo[b][1,4]dioxin-6-ol to replace 3-bromophenol, and 1-(diphenylmethyl)-1H-indole-2,3-dione to replace 1-((5-(trifluoromethyl)furan-2-yl)methyl)indoline-2,3-dione, 3-(7-chloro-6-hydroxy-2,3-dihydro-1,4-benzodioxin-5-yl)-1-(diphenylmethyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one was obtained (18%) as a colorless solid: MS (ES+) m/z 522.1 (M+23), 524.1 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415370B2
Source datasetuspto-grants-2013_04
ORD IDord-e37f5910cdb348f1bfaa196e20d0aff3
Source noteuspto-grants-2013_04