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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428159Generated: October 29, 2026

Ethylene Oxide → HCID 14472553, compound

https://huagongshe.com/reaction/428159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene OxideHCID 6354—
ReactantBoron trifluoride etherateHCID 8000—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Bromo-1,4-benzodioxineHCID 611440—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 14472553HCID 14472553—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3.73 g (17.5 mmol) of the compound obtained in Step A are dissolved in 90 ml of anhydrous tetrahydrofuran; the mixture is then cooled to −78° C. 16.4 ml (26.25 mmol) of n-butyllithium (1.6 M/hexane) are then slowly added to the solution; the reaction mixture is then stirred for 2 hours under argon at the same temperature. 2.2 ml (17.5 mmol) of boron trifluoride etherate and an excess of ethylene oxide are added in succession to the solution. After 30 minutes of stirring at −78° C., the reaction mixture is hydrolysed with a saturated ammonium chloride solution; the aqueous phase is then extracted with ethyl acetate. The organic phase, dried over magnesium sulphate and then filtered, is concentrated in vacuo. The title alcohol is obtained pure in the form of a clear oil after passage over a silica column (eluant:AcOEt/PE:20/80).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313160B1
Source datasetuspto-grants-2001_11
ORD IDord-4e018f0b1a244177a7d1353185c347d5
Source noteuspto-grants-2001_11