HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375764Generated: October 27, 2026
Ammonia → Methyl 4-methoxy-2,3-dihydro-1H-indole-2-carboxylate
https://huagongshe.com/reaction/2375764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Methoxy-1H-indole-2-carboxylic acid | HCID 907248 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Product | Methyl 4-methoxy-2,3-dihydro-1H-indole-2-carboxylate | HCID 22451269 | 64% |
Reaction Steps
119 mg (4.90 mmol) of magnesium turnings are added to a solution of 500 mg (2.44 mmol) of 4-methoxy-1H-indole-2-carboxylic acid in 10 ml of methanol. The mixture is stirred for 3 hours in a bath at 110° C. and then for 1 hour at room temperature. 20 ml of hydrochloric acid are added at 0° C. and the mixture is stirred for one hour. 3 N ammonia solution is then added to pH 10 and the mixture is extracted with 3 times 50 ml of ethyl acetate. The organic phases are dried over magnesium sulfate, filtered and concentrated under reduced pressure. The evaporation residue is purified by chromatography on a silica column using a dichloromethane/ethyl acetate mixture (98/5, then 95/5; v/v) as the eluent to give the expected product in the form of a brown oil with a yield of 64%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465811B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-e60a9ff312514d9fb42e07561a9f64af |
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| Source note | uspto-grants-2008_12 |
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