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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 243749Generated: October 28, 2026

Ammonium Chloride → HCID 86653809, compound

https://huagongshe.com/reaction/243749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBromocyclopropaneHCID 78037—
ReactantMagnesiumHCID 5462224—
ReactantMethyl 4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-acetateHCID 13051081—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86653809HCID 8665380979%

Reaction Steps

An anhydrous THF (50 mL) solution of bromocyclopropane (8.3 mL) was added dropwise to a metal magnesium (2.5 g), while heating. After the termination of dropwise addition, an anhydrous THF (20 mL) was added thereto, and the mixture was refluxed under heating for an additional 2 hours. Thereafter, the reaction mixture was allowed to air-cool, and this solution was added dropwise to an anhydrous THF (30 mL) solution of methyl (4-oxo-4,10-dihydro-9-oxa-3-thiabenzo[f]azulen-6-yl)acetate (10.0 g) previously chilled in an ice bath. After stirring the mixture for 30 minutes, an aqueous saturated ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with an aqueous saturated sodium chloride solution, and thereafter dried over anhydrous sodium sulfate. The solvents were distilled off under a reduced pressure, and the residue obtained was purified by silica gel column chromatography (hexane-ethyl acetate=5:1), to give 9.0 g (79%) of the captioned compound as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653285B2
Source datasetuspto-grants-2014_02
ORD IDord-3aac4aea93524bc2a2e500c285891a92
Source noteuspto-grants-2014_02