Réaction #452441

Équation de réaction

2-naphthoyl chloride

9-Decen-1-yl acetate

Lithium diisopropylamide

→

desired product

9-decen-1-yl 3-(β-naphthyl)-3-oxo-propionate

Solvants

THF

THF

Conditions de réaction

Traitement

1. 1
   Autrefitted with a magnetic stirrer
2. 2
   workup.ADDITIONinternal thermometer, argon inlet, and addition funnel
3. 3
   workup.ADDITIONthe resulting solution added to the flask over 45 min
4. 4
   workup.ADDITIONOnce addition
5. 5
   TempératureThe mixture is warmed to -20° C.
6. 6
   workup.STIRRINGstirred at that temperature for 18 h
7. 7
   TempératureAfter warming to 0° C.
8. 8
   Autrethe mixture is quenched with 20% HCl (47 mL)
9. 9
   workup.ADDITIONThe mixture is poured into a separatory funnel
10. 10
    workup.ADDITIONcontaining ether (150 mL) and water (250 mL)
11. 11
    ExtractionThe aqueous layer is extracted with ether (150 mL)
12. 12
    LavageThe combined organic layers are washed with saturated NaHCO3 solution (2×100 mL), water (2×150 mL) and brine (150 mL)
13. 13
    Séchagedried over MgSO4
14. 14
    Filtrationfiltered
15. 15
    AutreThe solvent is removed by rotary evaporation
16. 16
    Autreto give an orange/red oil
17. 17
    AutreThe oil is purified by column chromatography (elution with 2% ethyl acetate/petroleum ether)
18. 18
    Autreto yield a colorless oil

Mode opératoire

Lithium diisopropylamide (79.8 mL of a 2.0 M solution, 0.160 mol) is placed into a 250 mL three-necked round-bottomed flask fitted with a magnetic stirrer, internal thermometer, argon inlet, and addition funnel. The flask is cooled to -78° C. 9-Decen-1-yl acetate (14.91 g, 0.075 mol) is dissolved in THF (5 mL) and the resulting solution added to the flask over 45 min. Once addition is complete, the mixture is stirred for an additional 15 min. before being treated with a solution of 2-naphthoyl chloride (13.80 g, 0.071 mol) dissolved in THF (25 mL) over 30 min. The mixture is warmed to -20° C. and stirred at that temperature for 18 h. After warming to 0° C., the mixture is quenched with 20% HCl (47 mL). The mixture is poured into a separatory funnel containing ether (150 mL) and water (250 mL). The aqueous layer is extracted with ether (150 mL). The combined organic layers are washed with saturated NaHCO3 solution (2×100 mL), water (2×150 mL) and brine (150 mL), dried over MgSO4 and filtered. The solvent is removed by rotary evaporation to give an orange/red oil. The oil is purified by column chromatography (elution with 2% ethyl acetate/petroleum ether) to yield a colorless oil having 1H and 13C NMR spectra consistent with the desired product.

Source