Reacción #2383788

Ecuación de reacción

hydrochloric acid

sodium

allyl alcohol

diallyl 3,3′-thiodipropionate

→

title compound

Rendimiento 42.3%

Allyl 4-hydroxy-5,6-dihydro-2H-thiopyrane-3-carboxylate

Rendimiento 42.3%

Disolventes

water

diethyl ether

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.ADDITIONwas slowly added
2. 2
   OtroThe obtained reaction mixture
3. 3
   workup.STIRRINGThe mixture was stirred for another day at room temperature
4. 4
   workup.STIRRINGit was stirred until the whole
5. 5
   workup.DISSOLUTIONwas dissolved
6. 6
   OtroThe phases were separated
7. 7
   LavadoThe obtained organic phase was washed with water (400 ml)
8. 8
   SecadoThe organic phase was dried with magnesium sulfate
9. 9
   Filtraciónthe drying agent was filtered off
10. 10
    Otrothe filtrate was evaporated
11. 11
    Otrodried

Procedimiento

To a mixture of sodium sand (23 g; 1.0 mole) (Vogel's Textbook of Practical Organic Chemistry, Fourth Ed., Longman, London, 1978, p. 313) and anhydrous diethyl ether (3.4 1), allyl alcohol (65.8 ml) was slowly added. The obtained reaction mixture was stirred for two days at room temperature and then diallyl 3,3′-thiodipropionate (129.0 g; 0.5 mole) prepared according to the process disclosed in Example 1 was slowly added drop by drop. The mixture was stirred for another day at room temperature and then under ice cooling first absolute ethanol (10 ml) and then water (400 ml) and concentrated hydrochloric acid (455 ml) were added and it was stirred until the whole was dissolved. The phases were separated. The obtained organic phase was washed with water (400 ml), a 7% sodium hydrogencarbonate solution (3×400 ml) and once more with water (200 ml). The organic phase was dried with magnesium sulfate, the drying agent was filtered off, the filtrate was evaporated and dried. The title compound (42.4 g; 42%) was obtained as a crude product in the form of a yellowish oil.

Fuente