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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531992Generated: October 30, 2026

Ethyl Acetate → HCID 22247351, compound

https://huagongshe.com/reaction/1531992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant1-IodooctaneHCID 12380—
ReactantSodium hydrideHCID 24758—
ReactantHCID 69628847HCID 69628847—
SolventDimethylformamideHCID 6228—
ProductHCID 22247351HCID 22247351—

Reaction Steps

5-Bromo-7-methyl-7-nitroindoline (3.6 g) was dissolved in N,N-dimethylformamide (36 ml), and sodium hydride (677 mg) was added, which was followed by stirring at room temperature for 0.5 hr. 1-Iodooctane (3.4 g) was added to the reaction mixture and the mixture was stirred at the same temperature for 24 hr. Ethyl acetate (200 ml) was added to the reaction mixture, and the mixture was washed with water and dried over anhydrous sodium sulfate. Ethyl acetate was evaporated under reduced pressure. The residue was purified by gel column chromatography (eluent: ethyl acetate/n-hexane=1/100−1/50) to give 4.0 g of oily 1 -octyl-5-bromo-6-methyl-7-nitroindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200988B1
Source datasetuspto-grants-2001_03
ORD IDord-360539f620a94ea08b57346e5faa13e2
Source noteuspto-grants-2001_03