Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257571Generated: October 31, 2026

Dimethylformamide → HCID 54479667, compound

https://huagongshe.com/reaction/2257571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-1-(tetrahydropyran-2-yloxy)indaneHCID 54485916—
ReactantHCID 178418244HCID 178418244—
SolventDiethyl EtherHCID 3283—
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 tetrahydrofuran under a nitrogen atmosphere. To the solution was dropwise added 20 ml of a 1.5N n-butyllithiumhexane 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 numberUS05658904
Source datasetuspto-grants-1997_08
ORD IDord-97401f9517b04598a88e4911fd8f2f51
Source noteuspto-grants-1997_08