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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 641437Generated: October 31, 2026

Ethyl bromoacetate → HCID 66636183, compound

https://huagongshe.com/reaction/641437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium hydrideHCID 24758—
ReactantHCID 57426223HCID 57426223—
SolventDimethylformamideHCID 6228—
ProductHCID 66636183HCID 66636183—

Reaction Steps

Sodium hydride (45 mg of a 60% dispersion in mineral oil, 1.13 mmol) was added to a solution of ethyl (2-isopropyl-4-nitro-1H-indol-3-yl)acetate from Step E (300 mg, 1.03 mmol) in DMF (10 mL). After 5 min, ethyl bromoacetate (0.126 mL, 1.13 mmol) was added dropwise and the reaction mixture was stirred at ambient temperature for 30 min. The reaction mixture was quenched with saturated aqueous NaHCO3 (10 mL) and extracted with CHCl3 (3×25 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CHCl3:MeOH—100:0 to 95:5, to give the title compound. MS: m/z=377 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696192B2
Source datasetuspto-grants-2010_04
ORD IDord-2ff8d4da748749afbd630699e9d567d8
Source noteuspto-grants-2010_04