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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455884Generated: November 3, 2026

Hydrochloric Acid → HCID 22105421, compound

https://huagongshe.com/reaction/1455884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAnisoleHCID 7519—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 54293415HCID 54293415—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 22105421HCID 22105421—

Reaction Steps

To an ice-cooled suspension of aluminum trichloride (0.400 g; 0.003 mole) in methylene chloride (15 mL) in a nitrogen stream a solution of 2-methoxy-3,3-dibromo-alpha-(1-methylethylidene)-4-oxo-1-azetidine acetic acid benzyl ester (0.447 g; 0.001 mole) and anisole (0.648 g; 0.65 mL, 0.006 mole) in methylene chloride (15 mL) was added and then it was stirred for half an hour at room temperature. Ethyl acetate (15 mL) and 0.1N hydrochloric acid (5 mL) were added to the reaction mixture and the layers were separated. The ethyl acetate layer was extracted with a 5% sodium hydrogen carbonate solution (2×20 mL) and the layers were separated. The aqueous layer was acidified with 0.1N hydrochloric acid to pH 1, then fresh ethyl acetate (20 mL) and sodium chloride were added and the layers were again separated. The ethyl acetate layer was washed with a saturated salt solution, dried and evaporated to a dry residue to obtain 3,3-dibromo-2-methoxy-alpha-(1-methylethylidene)-4-oxo-1-azetidine acetic acid, which was identical to the one disclosed under 2a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843939
Source datasetuspto-grants-1998_12
ORD IDord-f48a411754e244feb239ddcc35550ac7
Source noteuspto-grants-1998_12