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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22933Generated: October 26, 2026

N,N-Dimethylaniline → 2-Phenylindole

https://huagongshe.com/reaction/22933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantBromomethyl 4-methoxyphenyl ketoneHCID 4965—
ReactantP-AnisidineHCID 7732—
SolventEthyl AcetateHCID 8857—
Product2-PhenylindoleHCID 13698—

Reaction Steps

To a boiling mixture of in-anisidine (1.56 ml, 20.0 minol) and N,N-dimethylaniline (3.5 ml) was added 2-bromo-4-methoxyacetophenone (1.37 g in EtOAc, 6.00 mmol) slowly by syringe. After addition, the mixture was kept at 170° C. for 1 hour. The reaction mixture was cooled to room temperature and a dark colored solid was formed. EtOAc was added along with HCI (2 N). The aqueous layer was extracted with EtOAc several times. The combined organic layers were washed with brine, and dried over MgSO4. Solvent was removed under the reduced pressure to afford a dark brown colored solid. Purification by recrystallization in EtOH afforded indole 31 as a white crystallinc material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849656B1
Source datasetuspto-grants-2005_02
ORD IDord-71e649dc94b4468a9952da8d86e5f34c
Source noteuspto-grants-2005_02