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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255184Generated: October 30, 2026

Isobutyl iodide → 7-fluoro4-isobutyl-2H-1,4-benzoxazin-3(4H)-one

https://huagongshe.com/reaction/2255184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl iodideHCID 10556—
ReactantSodium hydrideHCID 24758—
Reactant7-fluoro-3,4-dihydro-2H-1,4-benzoxazin-3-oneHCID 13731295—
SolventDimethylformamideHCID 6228—
Product7-fluoro4-isobutyl-2H-1,4-benzoxazin-3(4H)-oneHCID 1904716465%

Reaction Steps

To 3.96 g (99 mmol) of hexanes washed 60% sodium hydride in 150 ml of N,N-dimethylformamide was added portionwise as a solid 15 g (90 mmol) of 7-fluoro-2H-1,4-benzoxazin-3(4H)-one. When the addition was complete the reaction was stirred at room temperature for 10 min, after which time 19.8 g (108 mmol) of isobutyl iodide was added. The reaction was then stirred overnight before quenching onto 200 ml of water. The aqueous phase was extracted with EtOAc (2×150 ml) and the combined organics were dried over Na2SO4, filtered and evaporated in vacuo to give the desired alkylated product, as a yellow oil (13 g, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05238908
Source datasetuspto-grants-1993_08
ORD IDord-96fa3999b9b647e2923fb0aa70ddfb65
Source noteuspto-grants-1993_08