Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437320Generated: October 31, 2026

1,2-Dibromo-1,1,2,2-tetrafluoroethane → 8-Bromo-2,3-dihydro[1,4]dioxino[2,3-b]pyridine

https://huagongshe.com/reaction/1437320

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dibromo-1,1,2,2-tetrafluoroethaneHCID 31301—
Reactant2,3-Dihydro-1,4-dioxino[2,3-b]pyridineHCID 11007968—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product8-Bromo-2,3-dihydro[1,4]dioxino[2,3-b]pyridineHCID 68702454—

Reaction Steps

A solution of 2,3-dihydro-[1,4]dioxino[2,3-b]pyridine (prepared by the method of H. Neunhoffer et al, Chem., Ber., 1990, 123 (12), 2453) (1.37 g, 10 mmol) in tetrahydrofuran (20 ml) under argon at −78° C. was treated over 15 minutes with a solution of n-butyl lithium (20 mmol) in tetrahydrofuran (8 ml). After 30 minutes a solution of 1,2-dibromo-1,1,2,2-tetrafluoro-ethane (2.6 g, 10 mmol) in tetrahydrofuran (10 ml) was added dropwise over 5 minutes. After a further 30 minutes the cooling bath was removed and saturated aqueous ammonium chloride (20 ml) and ether (20 ml) were added. The mixture was allowed to warm to room temperature then partitioned between ether/water. The organic extract was washed with half-saturated brine, dried and evaporated. The residue was chromatographed on silica eluting with a 0-30% gradient of ethyl acetate in dichloromethane affording a yellow solid (1.1 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622481B2
Source datasetuspto-grants-2009_11
ORD IDord-992bb7f1196b40b48075b54466db89d6
Source noteuspto-grants-2009_11