Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441449Generated: October 27, 2026

Hexane → 3-(3-Chlorophenyl)-alpha-(4-fluorophenyl)-2,1-benzisoxazole-5-methanol

https://huagongshe.com/reaction/1441449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant4-FluorobenzaldehydeHCID 68023—
Reactant5-Bromo-3-(3-chlorophenyl)-2,1-benzisoxazoleHCID 12016670—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Chlorophenyl)-alpha-(4-fluorophenyl)-2,1-benzisoxazole-5-methanolHCID 1797610526.8%

Reaction Conditions

Temperature-70 °C

Reaction Steps

nBuLi 1.6M in hexane (0.112 mol) was added dropwise at −70° C. under N2 flow to a mixture of 5-bromo-3-(3-chlorophenyl)-2,1-benzisoxazole (0.097 mol) in THF (300 ml). The mixture was stirred at −70° C. for 15 min. A mixture of 4-fluoro-benzaldehyde (0.112 mol) in THF (100 ml) was added dropwise. The mixture was stirred at −70° C. for 30 min, then hydrolized and extracted with EtOAc. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated till dryness. The residue was taken up in diethyl ether and DIPE. The precipitate was filtered off, washed and dried, yielding 9.2 g (26.8%) of 3-(3-chlorophenyl)-α-(4-fluorophenyl)-2,1-benzisoxazole-5-methanol (intermediate 1), mp. 171° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655654B2
Source datasetuspto-grants-2010_02
ORD IDord-3a4d4e958a64463887f265702748cd9f
Source noteuspto-grants-2010_02