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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453524Generated: October 30, 2026

Hexane → HCID 58844048, compound

https://huagongshe.com/reaction/1453524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantMethacryloyl chlorideHCID 13528—
ReactantHCID 66856532HCID 66856532—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
ProductHCID 58844048HCID 58844048—

Reaction Steps

1-ethyl-2-methoxycyclohexanol from the previous step (10 g, 0.063 mole) in 50 ml ether was placed in a three neck flask equipped with a water condenser, addition funnel and a nitrogen inlet. This solution was cooled in an ice/water bath and n-butyllithium, 1.6 molar in hexane (45 ml, 0.072 mole) was added dropwise. The contents were allowed to warm to room temperature and stirred for 30 minutes. The mixture was cooled again in ice/water bath and methacryloyl chloride (7.31 g, 0.070 mole) in 25 ml ether was added dropwise and heated to reflux for 30 minutes. The reaction mixture was cooled to room temperature and quenched with 125 ml of deionized water. The organic phase was separated and the water phase was extracted with 50 ml ether. The combined ether solutions were washed with 100 ml brine and dried over anhydrous magnesium sulfate. The solvent was removed in a rotary evaporator and the crude product was chromatographed on a neutral alumina column using hexane as elutant. The product was a clear liquid (9.79 g) which was characterized by NMR and IR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476492B2
Source datasetuspto-grants-2009_01
ORD IDord-ba5d1f778ce44ced9e7df2802aeb41b3
Source noteuspto-grants-2009_01