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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399265Generated: October 30, 2026

Trifluoroacetic anhydride → 5-Chloro-6-(2-dimethylaminoethoxy)-1H-indole

https://huagongshe.com/reaction/399265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantPotassium CarbonateHCID 11430—
ReactantN-[4-Chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetalHCID 57027129—
SolventMethanolHCID 887—
SolventTrifluoroacetic acidHCID 6422—
Product5-Chloro-6-(2-dimethylaminoethoxy)-1H-indoleHCID 5408642277.5%

Reaction Steps

A solution of N-[4-chloro-3-(2-dimethylaminoethoxy)phenyl]aminoacetaldehyde dimethyl acetal (D7, 0.61 g, 0.002 mol) in TFA (2.6 ml) at 0° C., was treated with TFAA (2.6 ml) under an argon atmosphere. More TFA (3.7 ml ) was added and the reaction was heated to reflux for 48 h. The solution was evaporated to dryness and the residue taken up in EtOAc. The extract was dried (Na2SO4) and concentrated in vacuo to leave a brown oil which was dissolved in MeOH (10 ml), treated with K2CO3 (1 g) and then stirred at room temperature for 3 h The mixture was concentrated in vacuo, and then the residue treated with water and extracted with EtOAc. The solution was dried (Na2SO4) and concentrated in vacuo to give the title compound as a brown solid (0.37 g , 76%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817833
Source datasetuspto-grants-1998_10
ORD IDord-9226eaef93244376b2c927ac898b39ae
Source noteuspto-grants-1998_10