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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453854Generated: November 1, 2026

Methyl iodide → Methyl 4-chloro-1,2-dimethyl-1H-indole-3-carboxylate

https://huagongshe.com/reaction/453854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactantmethyl 4-chloro-2-methyl-1H-indole-3-carboxylateHCID 59473719—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
ProductMethyl 4-chloro-1,2-dimethyl-1H-indole-3-carboxylateHCID 5947366872%

Reaction Steps

Methyl 4-chloro-2-methyl-1H-indole-3-carboxylate (13.45 mmol, 1.0 equiv.) was dissolved in DMF (7 ml) and added at 0° C. to a suspension of NaH (26.90 mmol, 2.0 equiv.) in DMF (13 ml). The mixture was then stirred for 30 min. Methyl iodide (20.17 mmol, 1.5 equiv.) was added dropwise at 0° C. and stirring was carried out for 2 h at 25° C. The reaction mixture was diluted with NH4Cl solution (20 ml) and extracted with ethyl acetate (3×50 ml). The combined organic phases were washed with water and sat. NaCl solution (in each case 50 ml), dried over Na2SO4 and concentrated to dryness under reduced pressure. Yield: 72%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-7daa7349e05845bdb1ec6c47cb131807
Source noteuspto-grants-2013_07