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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108748Generated: October 30, 2026

Nitric Acid → HCID 22627413, compound

https://huagongshe.com/reaction/1108748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantHCID 22627144HCID 22627144—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 22627413HCID 22627413—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyl 1-(2-chlorobenzyl)-2-propylindole-6-carboxylate (200 mg) in trifluoroacetic acid (2 ml) was added concentrated nitric acid (0.3 ml) at 0° C. After stirred at 0° C. for 30 minutes, the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with aqueous sodium bicarbonate, water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by preparative thin layer chromatography on silica gel eluting with a mixture of ethyl acetate and hexane (1:3) to give methyl 1-(2-chlorobenzyl)-3-nitro-2-propylindole-6-carboxylate (73 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069156
Source datasetuspto-grants-2000_05
ORD IDord-8cb1e0ada0174951a2ed3a9187655474
Source noteuspto-grants-2000_05