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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382563Generated: November 1, 2026

6-Bromo-2,2-dimethyl-2H-chromene → 2-(4-benzyloxy-3,5-dimethoxy-phenyl)-1-(2,2-dimethyl-2H-chromen-6-yl)-ethanone

https://huagongshe.com/reaction/2382563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-2,2-dimethyl-2H-chromeneHCID 11770533—
Reactant(4-Benzyloxy-3,5-dimethoxy-phenyl)-acetaldehydeHCID 57436872—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product2-(4-benzyloxy-3,5-dimethoxy-phenyl)-1-(2,2-dimethyl-2H-chromen-6-yl)-ethanoneHCID 5755843020%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cooled (−78° C.) stirring solution of 6-bromo-2,2-dimethyl-2H-chromene, which was prepared according to Chemistry and Biology, 2000, Vol. 7, p. 979, (567.7 mg, 2.38 mmol) in THF (7 mL) was added n-BuLi (2.88 M, 0.94 mL, 2.71 mmol). After completion of addition, the reaction mixture continued to stir at −78° C. After 25 minutes, (4-benzyloxy-3,5-dimethoxy-phenyl)-acetaldehyde (619.6 mg, 2.17 mmol) dissolved in THF (7.0 mL) was added. After completion of addition the reaction continued to stir for 15 minutes and was then quenched with saturated ammonium chloride. The aqueous layer was separated and extracted with ethyl acetate. All Combined organic layers were dried over sodium sulfate, filtered, and concentrated to yield a crude oil. The crude material was purified by silica gel chromatography (3:1 ethyl acetate:hexanes) to yield the desired product (200.5 mg, 20% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263042B2
Source datasetuspto-grants-2012_09
ORD IDord-76f1d8eaed294545891c3f68f565cb2c
Source noteuspto-grants-2012_09