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ChemicalBook CAS DataBase List 2-[(1R)-2-HYDROXY-1-METHYLETHYL]-1H-ISOINDOLE-1,3(2H)-DIONE

2-[(1R)-2-HYDROXY-1-METHYLETHYL]-1H-ISOINDOLE-1,3(2H)-DIONE synthesis

4synthesis methods
35320-23-1 Synthesis
(R)-(-)-2-Amino-1-propanol

35320-23-1
448 suppliers
$8.00/5g

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Yield:73323-91-8 91%

Reaction Conditions:

with triethylamine in toluene; for 20 h;Reflux;

Steps:

21

A solution of R-alaminol (4.4 g, 58.6 mmol), phthalic anhydride (8.7 g, 58.6 mmol) and TEA (2.73 mL, 20 mmol) in 100 mL of toluene was heated at reflux with azeotropic removal of H2O with a Dean-Stark trap for 20 h. The solution was concentrated under reduced pressure. To the resulting residue was added 5 mL ether. When crystallization was complete, the solid was collected, washed with 5 mL hexanes and dried under vacuum to afford 2-((R)-2-hydroxy-1-methyl-ethyl)isoindole-1,3-dione (10.96 g, 91%).

References:

US2012/157494,2012,A1 Location in patent:Page/Page column 27-28

35320-23-1 Synthesis
(R)-(-)-2-Amino-1-propanol

35320-23-1
448 suppliers
$8.00/5g

22509-74-6 Synthesis
N-Carbethoxyphthalimide

22509-74-6
237 suppliers
$9.00/5g

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