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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362980Generated: October 30, 2026

Diethyl Ether → HCID 54479667, compound

https://huagongshe.com/reaction/362980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-1-(tetrahydropyran-2-yloxy)indaneHCID 54485916—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54479667HCID 54479667—

Reaction Steps

8.1 g of 5-bromo-1-(tetrahydropyran-2-yloxy)indane was dissolved in 100 ml of anhydrous tetra-hydrofuran under a nitrogen atmosphere. To the solution was dropwise added 20 ml of a 1.5N n-butyllithium-hexane solution at -65° C. in 10 minutes. The resulting mixture was stirred at the same temperature for 5 minutes. Thereto was added 2.3 ml of anhydrous N,N-dimethylformamide. The reaction mixture was heated to room temperature and added to a mixture of 100 ml of ice water, 100 ml of diethyl ether and 2 g of ammonium chloride. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant: toluene/ethyl acetate=15/1) to obtain 6.5 g of 5-formyl-1-(tetrahydropyran-2-yloxy)indane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05872117
Source datasetuspto-grants-1999_02
ORD IDord-1626f38630d84bbca2d9af7fe93f1055
Source noteuspto-grants-1999_02