Tetrahydrofuran → HCID 21288122, compound

To a suspension of 104 g (0.291 moles) of methyltriphenylphosphonium bromide in 100 ml dry tetrahydrofuran at 0° was added 115 ml (0.275 moles) of 2.4M n-butyllithium and the dark red solution was stirred at 0° for 30 minutes. Then a solution of 38.2 g (0.195 moles) of 2-(3-oxapropyloxy)-5-methoxybenzaldehyde in 100 ml of dry tetrahydrofuran was added and the solution was stirred at room temperature for 60 minutes. The solution was concentrated and the residue partitioned between ether and water. The ether layer was washed with aqueous Na2CO3, then brine, then dried (Na2SO4) and concentrated. The oily residue was dissolved in 500 ml of 10% ethylacetate-hexane and cooled at 0° overnight, then filtered. The filtrate was concentrated to give 33.8 g (89%) of 2-ethenyl-4-methoxy-1-O-methoxymethylphenol as a pale yellow liquid.

1. stirringthe solution was stirred at room temperature for 60 minutes
2. concentrationThe solution was concentrated
3. customthe residue partitioned between ether and water
4. washThe ether layer was washed with aqueous Na2CO3
5. dry with materialbrine, then dried (Na2SO4)
6. concentrationconcentrated
7. dissolutionThe oily residue was dissolved in 500 ml of 10% ethylacetate-hexane
8. temperaturecooled at 0° overnight
9. filtrationfiltered
10. concentrationThe filtrate was concentrated

ORD record

ord-ac7a92608b5a4bb997c4e27c74f6fabb

Source dataset

uspto-grants-1987_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04686235