反応 #1684

反応方程式

Cbz-D-hPro-OH

2,4,5-trichlorophenol

Pro-OH

triethylamine

1,3-dicyclohexylcarbodiimide

→

Cbz-D-hPro-Pro-OH

溶媒

ethyl acetate

反応条件

後処理

1. 1
   workup.ADDITIONAdded to the solution
2. 2
   ろ過The precipitate was filtered
3. 3
   濃縮the filtrate concentrated in vacuo to an oil
4. 4
   workup.DISSOLUTIONThe oil was dissolved in pyridine (100 mL)
5. 5
   workup.STIRRINGThe reaction was stirred at room temperature (24 hours)
6. 6
   その他The reaction solvent was removed in vacuo to an oil
7. 7
   workup.DISSOLUTIONThe residue was dissolved in water (100 mL)
8. 8
   workup.ADDITIONdiethyl ether (50 mL) was added
9. 9
   抽出The aqueous layer extracted twice with diethyl ether
10. 10
    その他The aqueous layer separated
11. 11
    workup.ADDITIONwas added
12. 12
    その他The organic layer was separated
13. 13
    乾燥dried (MgSO4)
14. 14
    その他the filtrate evaporated in vacuo to an amorphous solid (11.4 g, 88%)

実験手順

Cbz-D-hPro-OH (9.5 g, 36 mmol) was dissolved in ethyl acetate (100 mL) and the solution cooled to 0° C. Added to the solution was 2,4,5-trichlorophenol (7.1 g, 36 mmol) and 1,3-dicyclohexylcarbodiimide (7.4 g, 36 mmol). The reaction was stirred for 1 hour at 0° C. and 1 hour at room temperature. The precipitate was filtered and the filtrate concentrated in vacuo to an oil. The oil was dissolved in pyridine (100 mL), Pro-OH (4.2 g, 36 mmol), and triethylamine (5.0 mL, 36 mmol) were added. The reaction was stirred at room temperature (24 hours). The reaction solvent was removed in vacuo to an oil. The residue was dissolved in water (100 mL), diethyl ether (50 mL) was added and the pH adjusted to 9.5 with 2N sodium hydroxide. The aqueous layer extracted twice with diethyl ether. The aqueous layer separated, the pH adjusted to 2.8 with 3N hydrochloric acid and ethyl acetate (150 mL) was added. The organic layer was separated, dried (MgSO4), and the filtrate evaporated in vacuo to an amorphous solid (11.4 g, 88%).

出典