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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | N-[3-(2-dimethylaminoethoxy)4-methoxyphenyl]aminoacetaldehyde dimethyl acetal | HCID 10590199 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2-((5-Methoxy-1H-indol-6-yl)oxy)-N,N-dimethylethan-1-amine | HCID 10537659 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05889022 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-ec2a368294d64b0099dac7dd99712744 |
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| Source note | uspto-grants-1999_03 |
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