HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543203Generated: October 31, 2026
N,N-Dimethylaniline → 6-Methoxy-2-(4-methoxyphenyl)-1H-indole
https://huagongshe.com/reaction/543203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Methoxyaniline | HCID 10824 | — |
| Product | 6-Methoxy-2-(4-methoxyphenyl)-1H-indole | HCID 12398998 | — |
Reaction Steps
A solution of 33 grams (0.16 mole) of 4-methoxy-bromacetophenone in 230 ml of xylene was dropped into a mixture of 54.5 grams (0.45 mole) of m-anisidine and 76 ml of N,N-dimethyl aniline which was heated to 170° C. bath temperature. After cooling the mixture was treated with ethyl acetate and extracted by shaking with 2N HCl. The aqueous phase was again terated with ethyl acetate and the combined organic phases extracted by shaking several times with 2N HCl. After washing with water and drying the solvent was removed in a vacuum. The crystalline residue was washed colorless with a little ethyl acetate. Yield: 18.8 grams, M.P. 228°-230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04661511 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-45fde2f603734c198db5c36a5afb9da2 |
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| Source note | uspto-grants-1987_04 |
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