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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486513Generated: October 28, 2026

Ammonium Chloride → HCID 2757493, compound

https://huagongshe.com/reaction/486513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
Reactant2-(2-Bromoethyl)-1,3-dioxolaneHCID 87776—
ReactantMagnesium ChlorideHCID 5360315—
ReactantMagnesiumHCID 5462224—
Catalystcopper(I) bromideHCID 24593—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 2757493HCID 275749334%

Reaction Conditions

Temperature23 °C

Reaction Steps

2-(2-Bromoethyl)-1,3-dioxolane (40 ml) was added dropwise within 15 minutes under argon and while stirring at a maximum 30° C. to a suspension of Rieke magnesium, prepared from 44.9 g of magnesium chloride, in 1500 ml of absolute tetrahydrofuran. The suspension was stirred at room temperature (about 23° C.) for 15 minutes, cooled to 0° C. and, after the addition of 43.5 g of copper(I) bromide, stirred at 5° C. for 15 minutes. After cooling to -70° C. 33 ml of 3-chlorobenzoyl chloride were added dropwise within 10 minutes. The reaction mixture was stirred at -70° C. for 15 minutes and at room temperature for 2 hours and subsequently hydrolyzed with 1000 ml of saturated ammonium chloride solution while cooling at a maximum 20° C. After the addition of 500 ml of water the mixture was extracted three times with 1000 ml of ethyl acetate each time. The combined organic extracts were washed with 1000 ml of saturated sodium chloride solution, dried over MgSO4 and freed from solvent. 59.2 g of oil were chromatographed on 1500 g of silica gel with ethyl acetate/hexane (1:3) as the eluent. 20.9 g (34%) of 3'-chloro-3-(1,3-dioxolan-2-yl)propiophenone were isolated as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292732
Source datasetuspto-grants-1994_03
ORD IDord-00f997e68bc8479b9361dca063086f75
Source noteuspto-grants-1994_03