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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502915Generated: November 4, 2026

Hexane ethyl acetate hexane → 3-Bromo-1,5-dimethyl-4-isopropoxy-8-oxa-bicyclo[3.2.1]octa-3,6-dien-2-one

https://huagongshe.com/reaction/502915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexane ethyl acetate hexaneHCID 21939919—
ReactantMonosodium phosphateHCID 23672064—
ReactantLithium propan-2-olateHCID 23673350—
Reactant3,4-Dibromo-1,5-dimethyl-8-oxa-bicyclo[3.2.1]octa-3,6-dien-2-oneHCID 68462159—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-1,5-dimethyl-4-isopropoxy-8-oxa-bicyclo[3.2.1]octa-3,6-dien-2-oneHCID 5860953168%

Reaction Steps

A solution of 2.74 g (8.9 mmol) of 3,4-dibromo-1,5-dimethyl-8-oxa-bicyclo[3.2.1]octa-3,6-dien-2-one (prepared according to Organic Lett. 4(12), 1997 (2002)) dissolved in 10 ml of tetrahydrofuran is added dropwise at ambient temperature to a solution of 5.4 ml (10.7 mmol) of 2M lithium isopropanolate diluted with 10 ml of tetrahydrofuran. The mixture is stirred for 3 hours at ambient temperature until the starting material has reacted completely (TLC monitoring: hexane/ethyl acetate/hexane 4:1). The reaction solution is then treated at a temperature of 0° C. with a 10% sodium dihydrogen phosphate solution (20 ml) and water (30 ml) and extracted three times with ethyl acetate. Drying over sodium sulfate and concentration by evaporation are carried out. For further purification, the dark oil so obtained is purified by chromatography over silica gel with 5% ethyl acetate in hexane. 1.73 g (68% of theory) of pure 3-bromo-1,5-dimethyl-4-isopropoxy-8-oxa-bicyclo[3.2.1]octa-3,6-dien-2-one are isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776888B2
Source datasetuspto-grants-2010_08
ORD IDord-59a2ab5241494cfbb1d6a0df3482335f
Source noteuspto-grants-2010_08