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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873735Generated: October 30, 2026

6-bromo-2,2-dimethyl-4H-spiro[chromene-3,1'-cyclopropan]-4-one → 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,1'-cyclopropane]

https://huagongshe.com/reaction/873735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-bromo-2,2-dimethyl-4H-spiro[chromene-3,1'-cyclopropan]-4-oneHCID 86724277—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,1'-cyclopropane]HCID 8672428395%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of methyl(triphenyl)phosphonium bromide (20.8 g, 58.2 mmol) in tetrahydrofuran (168 ml) was added n-butyllithium (2.69 M solution in hexane, 21.6 ml, 58.2 mmol) under dry ice-acetone bath cooling and argon atmosphere. The mixture was stirred for 1 hour at 0° C. To the mixture was added 6-bromo-2,2-dimethyl-4H-spiro[chromene-3,1′-cyclopropan]-4-one (8.18 g, 29 mmol). The mixture was stirred for 1 hour at 0° C. The reaction was quenched by adding water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. The residue was purified by silicagel column chromatography (hexane/ethyl acetate=20:1-10:1) to afford 6-bromo-2,2-dimethyl-4-methylene-4H-spiro[chromene-3,1′-cyclopropane] (7.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975415B2
Source datasetuspto-grants-2015_03
ORD IDord-bad599bd1b8947e4a5346ebc245371a2
Source noteuspto-grants-2015_03