Diethyl Ether → HCID 70492662, compound

Temperature

0 °C

A 2 liter flask is charged with one equivalent of methyl triphenylphosphonium chloride and 600 ml. of anhydrous diethyl ether. This solution is cooled to 0° C. and one equivalent of n-butyllithium in hexane is introduced over a thirty minute period under nitrogen. When addition is complete, the solution is aged an additional 30 minutes at 0°-5° C. Then a solution of one equivalent of 2-formyl-3-acetoxy-4,5-diacetoxymethyl pyridine in 250 ml. of anhydrous ether is added dropwise with stirring over a one hour period. The reaction mixture is then aged 16 hours temperature, and is then cooled to 0° C. and filtered. The filtrate is concentrated to dryness under reduced pressure and treated with a mixture of 500 ml. of 2.5 N hydrochloric acid and 300 ml. of ethyl acetate. After shaking well, the organic phase is separated and discarded. The aqueous phase is extracted with 2 more 300 ml. portions of ethyl acetate and these too are discarded. The aqueous phase is then refluxed with stirring under nitogen for 3 hours and after cooling is poured onto excess aqueous sodium bicarbonate. The crude, solid, free base is isolated by filtration and air dried. This crude solid is taken up into 300 ml. dry tetrahydrofuran and saturated with dry hydrogen chloride at 0° C. Then 300 ml. dry diethyl ether is introduced and the desired hydrochloride crystallized. It is isolated by filtration and dried in vacuo.

1. additionWhen addition
2. temperatureaged 16 hours temperature, and is then cooled to 0° C.
3. filtrationfiltered
4. concentrationThe filtrate is concentrated to dryness under reduced pressure
5. additiontreated with a mixture of 500 ml
6. stirringAfter shaking well
7. customthe organic phase is separated
8. extractionThe aqueous phase is extracted with 2 more 300 ml
9. temperatureThe aqueous phase is then refluxed
10. stirringwith stirring under nitogen for 3 hours
11. temperatureafter cooling
12. additionis poured onto excess aqueous sodium bicarbonate
13. customThe crude, solid, free base is isolated by filtration and air
14. customdried
15. customat 0° C
16. additiondry diethyl ether is introduced
17. customthe desired hydrochloride crystallized
18. customIt is isolated by filtration
19. customdried in vacuo

ORD record

ord-c47522b2f5014730beaed080dd08184e

Source dataset

uspto-grants-1980_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04217352