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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130323Generated: October 31, 2026

Oxalyl chloride → 4,6-dimethoxy-2,3-dihydro-1H-indole-2,3-dione

https://huagongshe.com/reaction/130323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantBenzenamine, 3,5-dimethoxy-, hydrochloride (1:1)HCID 218603—
Product4,6-dimethoxy-2,3-dihydro-1H-indole-2,3-dioneHCID 11557522100%

Reaction Steps

12 g (63 mmol) of 3,5-dimethoxyaniline hydrochloride and 20 ml (230 mol) of oxalyl chloride were stirred at 165° C. for 30 min. The excess of oxalyl chloride was distilled (the color of the reaction mixture changed from dark-red to green-yellow). The reaction mixture was cooled and methanol was added. The resulting suspension was heated then filtered, washed with methanol and dried to yield 13 g of 4,6-dimethoxyindole-2,3-dione (100% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381730B2
Source datasetuspto-grants-2008_06
ORD IDord-37dc510889a84c359231f537edcf0396
Source noteuspto-grants-2008_06