反应详情

温度

0 °C

(1-Trityl-1H-imidazol-4-yl)acetic acid (65 g, 0.17 mol) is suspended in THF (400 mL) and cooled to 0° C. To this is added BH3.THF solution (350 mL, 1.0 M). The clear solution obtained is stirred at 0° C. for 30 min before warming to room temperature until LCMS indicated completion of the reaction. The solution is cooled again to 0° C. and quenched carefully with water (250 mL). The resulting solution is diluted with EtOAc (300 mL) and transferred to a separatory funnel and the aqueous layer is extracted with EtOAc. The organic phase is dried over anhydrous Na2SO4 and evaporated to give a sticky residue which is taken up in ethanolamine (800 mL) and heated to 90° C. for 2 h. The reaction is transferred to a separatory funnel, diluted with EtOAc (1 L) and washed with water (3×600 mL). The organic phase is dried over anhydrous Na2SO4 and evaporated to give 2-(1-trityl-1H-imidazol-4-yl)-ethanol as a white solid that is used as is without further purification. MS (ESI) m/z 354.8 (M+H) (prepared by alternate method in J. Med. Chem. 1996, 39(19), 3806)

1. customThe clear solution obtained
2. temperaturebefore warming to room temperature until LCMS
3. customcompletion of the reaction
4. temperatureThe solution is cooled again to 0° C.
5. customquenched carefully with water (250 mL)
6. additionThe resulting solution is diluted with EtOAc (300 mL)
7. customtransferred to a separatory funnel
8. extractionthe aqueous layer is extracted with EtOAc
9. dry with materialThe organic phase is dried over anhydrous Na2SO4
10. customevaporated
11. customto give a sticky residue which
12. temperatureheated to 90° C. for 2 h
13. customThe reaction is transferred to a separatory funnel
14. washwashed with water (3×600 mL)
15. dry with materialThe organic phase is dried over anhydrous Na2SO4
16. customevaporated