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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106661Generated: November 1, 2026

Ammonium Chloride → HCID 54030506, compound

https://huagongshe.com/reaction/2106661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBromocyclopropaneHCID 78037—
ReactantMethanone, (1-methyl-1H-pyrrol-2-yl)phenyl-HCID 142165—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54030506HCID 5403050660.5%

Reaction Steps

To a suspension of magnesium turnings (5.29 g, 0.22 mole) in anhydrous tetrahydrofuran (70 ml), cyclopropyl bromide (26.35 g, 0.22 mole) in tetrahydrofuran (50 ml) was added dropwise under nitrogen. The reaction mixture was heated at reflux for one h after the initial exotherm had subsided before (N-methylpyrrol-2-yl)phenylketone (13.3 g, 0.072 mole) (J. White and G. McGillivray, J. Org. Chem., (1977), 42, 4248, R. Greenhouse and C. Ramirez, J. Org. Chem., (1985), 50, 2961) in anhydrous tetrahydrofuran (50 ml ) was introduced dropwise. After heating the reaction mixture at reflux for 3 h it was cooled and saturated, aqueous ammonium chloride solution (95 ml) and water (150 ml) were added. The mixture was extracted with ethyl acetate (3×200 ml) and the combined extracts were dried (MgSO4). Flash chromatography of the residue on evaporation on silica gel eluting with heptane/tetrahydrofuran (9:1) provided the title compound as an oil (9.9 g, 46%) which solidified on standing. T.l.c. rf=0.35 (SiO2, heptane/THF (7:3)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931450
Source datasetuspto-grants-1990_06
ORD IDord-7d0c67b2149443dd865dce9f48155100
Source noteuspto-grants-1990_06