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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant4-Methoxy-1H-indole-2-carboxylic acidHCID 907248—
ReactantMagnesiumHCID 5462224—
ProductMethyl 4-methoxy-2,3-dihydro-1H-indole-2-carboxylateHCID 2245126964%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465811B2
Source datasetuspto-grants-2008_12
ORD IDord-e60a9ff312514d9fb42e07561a9f64af
Source noteuspto-grants-2008_12