Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

ChemicalBook CAS DataBase List Z-CIS-HYP-OH

Z-CIS-HYP-OH synthesis

13synthesis methods
-

Yield: 90.2%

Reaction Conditions:

with water;sodium hydroxide at 80; for 3 h;

Steps:

4 Reference Example 4
708 g of water and 337 g of 48% sodium hydroxide were added to 928 g of the crude product obtained in Reference Example 3, and the temperature was raised to 80 ° C., followed by reaction ripening for 3 hours. After completion of the aging, 146 g was distilled out under reduced pressure to 13 kPa under the same temperature condition. After concentration, the temperature was cooled to 20 ° C., 180 g of 48% caustic soda was added, and aging was carried out at 25 ° C. for 12 hours. The content of cis-benzyloxycarbonyl-4-hydroxy-L-proline in the reaction solution was 2.19 mol (the yield based on trans-4-hydroxy-L-proline was 81.0%). 35 g of toluene was added to the hydrolysis reaction solution, and the mixture was concentrated under reduced pressure at 7 kPa at 40 ° C. to distill off 332 g. To the concentrated solution, 161 g of concentrated sulfuric acid was added dropwise to adjust the pH to 1.3. After adjusting to acidity, 710 g of tetrahydrofuran and 354 g of water were added and the layers were separated. To the separated aqueous layer side, 356 g of tetrahydrofuran was added and the layers were separated. The separated tetrahydrofuran layer side was mixed and concentrated at 40 ° C. under 26 kPa reduced pressure to obtain 896 g of a concentrate (cis-benzyloxycarbonyl-4-hydroxy-L-proline 2.12 mol (yield 90. 2%), cis / trans = 98.3 / 1.7)

References:

TORAY FINE CHEMICALS COMPANY LIMITED;NISHIMURA, TOMOAKI;MORIMOTO, MASAO JP5703654, 2015, B2 Location in patent:Paragraph 0054; 0055

Z-CIS-HYP-OH Related Search: