Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253402Generated: October 30, 2026

Diethyl Ether → HCID 58086318, compound

https://huagongshe.com/reaction/253402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBromineHCID 24408—
ReactantMagnesiumHCID 5462224—
Reactant2,3-Bis-(4-chloro-benzyloxy)-benzaldehydeHCID 58087304—
SolventBenzeneHCID 241—
ProductHCID 58086318HCID 58086318—

Reaction Steps

To magnesium (0.098 g, turnings, 4.0 mmol) in a mixture of anhydrous ether (20 mL) and benzene (20 mL) at 0° C., bromine (0.10 mL, 2.0 mmol) was added dropwise. When the reaction had started, stirring was commenced and the addition of bromine continued until complete. The ice bath was removed and the reaction mixture was heated until the solution was almost colorless. After cooling down, the reaction mixture was slowly added to a solution of 2,3-bis-(4-chloro-benzyloxy)-benzaldehyde (62, 0.78 g, 2.0 mmol) in benzene (60 mL) at room temperature while stirring vigorously. Upon completion of the addition, the reaction mixture was stirred at room temperature overnight, then refluxed for 36 hours. After the reaction mixture was cooled down to room temperature, a solid was collected by filtration and washed with benzene, then boiled in hydrochloric acid (100 mL, 1.0 M) for 30 minutes. After cool down, the solution was extracted with dichloromethane. The organic layer was washed with brine and dried over magnesium sulfate. An off-white solid was obtained after removal of the solvent (63, 0.32 mg, 60%). MS (ESI) [M−H+]−=261.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872018B2
Source datasetuspto-grants-2011_01
ORD IDord-2b651b0a67044fef8ae3979cacdea873
Source noteuspto-grants-2011_01