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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057821Generated: November 1, 2026

1,2-Dichlorobenzene → 4-allyl-5-hydroxy-N-neopentylindole

https://huagongshe.com/reaction/1057821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
Reactant5-allyloxy-N-neopentylindoleHCID 18672460—
Product4-allyl-5-hydroxy-N-neopentylindoleHCID 18672464—

Reaction Steps

5-Allyloxy-N-neopentylindole (Step B; 1.4 g, 4.93 mmol) was refluxed in 20 mL 1,2-dichlorobenzene for 4 hours. The reaction mixture was cooled and immediately purified by flash chromatography on silica gel (gradient elution: hexane then 10% ethyl acetate/hexane) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515015B1
Source datasetuspto-grants-2003_02
ORD IDord-9c5ee24b9dfd4ffc8b14f8e6ac987a43
Source noteuspto-grants-2003_02