3-Phenylprop-2-Enal → HCID 54110718, compound

In an atmosphere of argon, 0.725 g (2.7 mmol) of (S)-2-[N-(3'-tert-butylsalicylidene)amino]-3-methyl-1-butanol, 2.5 ml of dichloromethane and 0.74 ml (2.45 mmol) of titanium tetraisopropoxide were placed in a schlenk tube, were stirred at room temperature over 1 hour and were cooled to -20° C. to prepare a dichloromethane solution. To the dichloromethane solution, 0.31 ml (2.45 mmol) of cinnamaldehyde and 1.0 ml (12.5 mmol) of diketene were added in this order, and were vigorously stirred at -20° C. over 48 hours. Subsequently, 0.23 ml (4.9 mmol) of isopropyl alcohol was added to the mixture and vigorously stirred at room temperature over 1 hour to give a reaction mixture. The reaction mixture was added to a mixed solution of 50 ml of 1N HCl and 50 ml of diethyl ether, and vigorously stirred at room temperature over 24 hours to give a solution. The solution was extracted with three portions of 50 ml of diethyl ether. The diethyl ether portions were combined, washed twice with 50 ml of a saturated sodium hydrogencarbonate aqueous solution, and further washed twice with 50 ml of a saturated sodium chloride aqueous solution to obtain a washed solution. To the solution, anhydrous magnesium sulfate was added to dry. The solvent of the solution was removed by distillation in vacuo to obtain a concentrated solution. The concentrated solution was placed on a silica gel column and eluted with a mixture of benzene and diethyl ether (benzene:diethyl ether=3:1) to give 0.58 g of optically active isopropyl 5-hydroxy-3-oxo-7-phenyl-6-heptenoate (yield: 86%; optical purity: 78% ee).

1. temperaturewere cooled to -20° C.
2. stirringwere vigorously stirred at -20° C. over 48 hours
3. stirringvigorously stirred at room temperature over 1 hour
4. customto give a reaction mixture
5. stirringvigorously stirred at room temperature over 24 hours
6. customto give a solution
7. extractionThe solution was extracted with three portions of 50 ml of diethyl ether
8. washwashed twice with 50 ml of a saturated sodium hydrogencarbonate aqueous solution
9. washfurther washed twice with 50 ml of a saturated sodium chloride aqueous solution
10. customto obtain a washed solution
11. customto dry
12. customThe solvent of the solution was removed by distillation in vacuo
13. customto obtain a concentrated solution
14. washeluted with a mixture of benzene and diethyl ether (benzene:diethyl ether=3:1)

ORD record

ord-c75dac9a60db43b699f01b51b8042afa

Source dataset

uspto-grants-1995_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05457225