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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419824Generated: October 25, 2026

Trifluoroacetic anhydride → 2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amine

https://huagongshe.com/reaction/1419824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantN-[3-(2-dimethylaminoethoxy)4-methoxyphenyl]aminoacetaldehyde dimethyl acetalHCID 10590199—
SolventTrifluoroacetic acidHCID 6422—
Product2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amineHCID 1053765983%

Reaction Steps

A stirred solution of N-[3-(2-dimethylaminoethoxy)-4-methoxyphenyl]aminoacetaldehyde dimethyl acetal (D15, 5.3 g, 0.018 mole) in trifluoroacetic acid (22 ml) at -5° C. under argon was treated dropwise over 40 minutes with trifluoroacetic anhydride (22 ml). After a further 30 minutes the dark solution was treated with more trifluoroacetic acid (33 ml) and then heated under reflux for 7 hours. The solution was concentrated in vacuo and the residue basified with 10% Na2CO3 solution and extracted with ethyl acetate. The extract was dried (Na2SO4), concentrated in vacuo and the residue dissolved in methanol (100 ml), treated with potassium carbonate (10 g) and stirred at room temperature for 3 hours. The mixture was concentrated in vacuo, the residue treated with water (60 ml) and extracted with ethyl acetate (2×70 ml). The combined extract was dried (Na2SO4) and concentrated in vacuo to afford the title compound as a brown solid (3.5 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05889022
Source datasetuspto-grants-1999_03
ORD IDord-ec2a368294d64b0099dac7dd99712744
Source noteuspto-grants-1999_03