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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192239Generated: October 30, 2026

Water → 6-Bromoindole

https://huagongshe.com/reaction/2192239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyrrolidineHCID 31268—
ReactantDimethylformamide dimethyl acetalHCID 78373—
Reactant4-Bromo-2-nitrotolueneHCID 123546—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
SolventDimethylformamideHCID 6228—
Product6-BromoindoleHCID 67649339.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a mixture solution of 4-bromo-2-nitrotoluene (2.00 g, 9.26 mmol) and dimethylformamide-dimethylacetal (3.68 mL, 27.8 mmol) in DMF (20 mL), pyrrolidine (1.16 mL, 13.9 mmol) was added at room temperature. After stirring at 110° C. for an hour, the mixture was cooled to room temperature and then water was added. After extracting 3 times with ether, the collected organic layer was dried with anhydrous magnesium sulfate and the concentrated. The resulting residue was subjected to the next reaction without purification. After adding 80% acetic acid aqueous solution (60 mL), the mixture was heated to 85° C. While adding zinc powder (5.27 g, 80.6 mmol) in small amounts, the mixture was stirred at 85° C. for 2 hours. After cooling to room temperature and filtering, followed by addition of water, the filtrate was extracted with ethyl acetate. The collected organic layer was washed with brine and concentrated by drying with anhydrous magnesium sulfate. The residue was purified by chromatography (silica gel, EA:Hx=1:20). The target compound (710 mg) was obtained as violet solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329708B2
Source datasetuspto-grants-2012_12
ORD IDord-85172445ba6748378df251619dea3cd5
Source noteuspto-grants-2012_12