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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527967Generated: October 31, 2026

Tetrahydrofuran → HCID 86656446, compound

https://huagongshe.com/reaction/527967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
ReactantQuinoxaline, 2,3-dichloro-6-fluoro-HCID 4447681—
ReactantHCID 12666545HCID 12666545—
Reactant1,2,2,3-TetramethylpiperidineHCID 18761772—
ReactantButyllithiumHCID 178418339—
SolventDimethylformamideHCID 6228—
ProductHCID 86656446HCID 8665644671%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of tetramethylpiperidine (16.4 mL) in dry THF (100 mL) was cooled to −78° C. and treated dropwise with n-BuLi (2.5M in Hex; 39 mL). The solution was further stirred at −78° C. for 30 min. A solution of 6-fluoro-2,3-dimethoxy-quinoxaline (15.6 g; prepared from the commercially available 2,3-dichloro-6-fluoroquinoxaline according to Egyptian Journal of Chemistry (1980), Volume Date 1977, 20, 427-39) in dry THF (450 mL) was cooled to −78° C., treated dropwise with the first solution and further stirred at −78° C. for 30 min. The resulting reaction mixture was treated with DMF (11.56 mL) and further stirred at −78° C. for 15 min. The reaction mixture was poured onto a mixture of a sat. NH4Cl solution and ice and extracted with ether. The org. layer was washed with brine, dried over MgSO4, evaporated under reduced pressure and crystallised from Hex/EA affording a light yellow solid (12.5 g; 71% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346804B2
Source datasetuspto-grants-2016_05
ORD IDord-afb133ca8512465889c03faec961d0d8
Source noteuspto-grants-2016_05