Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871940Generated: November 1, 2026

Tetrapropylammonium → HCID 18922186, compound

https://huagongshe.com/reaction/1871940

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrapropylammoniumHCID 9559—
Reactant2-PyridinecarboxaldehydeHCID 14273—
ReactantMethyl morpholine oxideHCID 82029—
Reactant5-Bromo-3,3-dimethyl-2,3-dihydro-1-benzofuranHCID 5323595—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 18922186HCID 1892218629%

Reaction Steps

To 1.0 g (3.5 mmol) of a stirring solution of 5-bromo-2,3-dihydro-3,3-dimethylbenzo[b]furan in 2.0 mL of ether and 18 mL of dry hexane at -78° C. is added 4.4 mL (7.1 mmol) of t-butylithium in hexane. The resulting mixture is stirred for 40 min, then 0.5 g (4.6 mmol) of 2-pyridinecarboxaldehyde is added. The reaction is allowed to slowly reach RT and is then quenched with water. The reaction is then diluted with 50 mL of ether, and the organic layer is separated. The remaining aqueous layer is extracted with ether (3×20 mL). The organic layers are then combined, dried over MgSO4, filtered, and the solvent was removed in vacuo. The residue is dissolved in 20 mL CH2Cl2, and to this solution was added 0.1 g (0.4 mmol) of tetrapropylammonium perruthinate followed by 0.6 g (5.3 mmol) of N-methyl morpholine-N-oxide at RT. The reaction is stirred for 3 h, then filtered through silica gel, and the solvent is removed in vacuo. Purification by sgc with 1 ethyl acetate:5 hexane resultes in about 0.30 g (29%) of a yellow solid. mp 95-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107311
Source datasetuspto-grants-2000_08
ORD IDord-fd1a13045ac84cc88829bfbcf5fce02f
Source noteuspto-grants-2000_08