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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453863Generated: October 29, 2026

Methyl 2-(bromomethyl)-6-methylbenzoate → ethyl 2-(6-(7-methyl-1-oxoisoindolin-2-yl)-1H-indol-1-yl)acetate

https://huagongshe.com/reaction/453863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 2-(bromomethyl)-6-methylbenzoateHCID 10263795—
ReactantEthyl 2-(6-amino-1H-indol-1-yl)acetateHCID 16731704—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
Productethyl 2-(6-(7-methyl-1-oxoisoindolin-2-yl)-1H-indol-1-yl)acetateHCID 5947365764%

Reaction Steps

Ethyl 2-(6-amino-1H-indol-1-yl)acetate (intermediate B) (7.66 mmol, 1 equiv.) was dissolved in benzene (30 ml), and methyl 2-(bromo-methyl)-6-methylbenzoate (8.42 mol, 1.1 equiv.) and TEA (9.19 mmol, 1.2 equiv.) were added at 25° C. and the mixture was refluxed for 12 h. The reaction mixture was reduced under reduced pressure and the residue was taken up in dichloromethane (30 ml), washed with water and sat. NaCl solution (5 ml), dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by column chromatography (10% ethyl acetate in hexane). Yield: 64%

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492559B2
Source datasetuspto-grants-2013_07
ORD IDord-15f20744fb304cf4ba7654645aa3c242
Source noteuspto-grants-2013_07