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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751402Generated: October 28, 2026

Heptane → 7-bromo-3,4-dihydro-2H-1-benzopyran-4-one

https://huagongshe.com/reaction/1751402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptaneHCID 8900—
Reactant7-Bromo-4H-1-benzopyran-4-oneHCID 18686752—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-3,4-dihydro-2H-1-benzopyran-4-oneHCID 2233573678.5%

Reaction Steps

A solution of diisobutylaluminum hydride in heptane (1.0 M, 60 mL, 60.0 mmol) was added dropwise to a solution of 7-bromo-4H-chromen-4-one (4.5 g, 20.0 mmol) in tetrahydrofuran at −78° C. under an atmosphere of argon over a period of 30 minutes. After 30 minutes the reaction was quenched with a mixture of silica gel (10 g), and water (10 mL). The mixture was allowed to warm to room temperature and was filter through celite and the tetrahydrofuran was removed under reduced pressure. The residue was taken up in chloroform (100 mL) and washed with sodium hydroxide (1N, 25 mL) and dried over sodium sulfate. The mixture was filtered and the solvent was removed under reduced pressure. The residue was subjected to flash chromatography with eluant of dichloromethane. The product containing fractions were combined and the solvent was removed under reduced pressure to provide 7-bromochroman-4-one (3.57 g, 15.7 mmol, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-2e62a9abe9414b9baf9a2f74f020e7b8
Source noteuspto-grants-2015_10