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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110868Generated: November 3, 2026

Diethyl Ether → HCID 54370108, compound

https://huagongshe.com/reaction/1110868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantSodium hydrideHCID 24758—
ReactantBenzene, 1-iodo-3-methoxy-HCID 69839—
Reactant2H-Indol-2-one, 3-[(dimethylamino)methylene]-1,3-dihydro-, (Z)-HCID 3028974—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
ProductHCID 54370108HCID 54370108—

Reaction Steps

In a flame dried flask under nitrogen, sodium hydride (50% dispersion in oil, 0.96 g, 20 mmoles) was washed free of oil with hexane. Dry dimethylformamide (DMF, 50 ml) and 3-(dimethylaminomethylene)-2(1H,3H)-indolone [Chem. Ber. 85:774 (1952); 3.77 g, 20 mmoles] were added, and the mixture stirred for 30 minutes (until gas evolution ceased). m-Iodoanisole (9.36 g, 40 mmoles) in 20 ml DMF was added, followed by Cu2Br2 (5.74 g, 20 mmoles). The reaction mixture was heated at 120°-130° for 40 hours, poured over 300 g of ice, stirred with 300 ml ether, filtered and the ether layer separated, dried over MgSO4, filtered and concentrated to an oil. The oil was chromatographed on silica gel, using ethyl acetate as eluant and title product initially isolated as an oil, crystallized from ether, 2.46 g (42%), m.p. 106°-108.5° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977178
Source datasetuspto-grants-1990_12
ORD IDord-265938f88c474ac9878653bccf2a90ab
Source noteuspto-grants-1990_12