反应 #1244308

反应方程式

tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate

tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate

Imidazole

Iodine

Triphenylphosphine

→

tert-butyl (2R)-2-fluoro-3-iodopropylcarbamate

收率 68.9%

溶剂

methylene chloride

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   温度cooled to 0° C
2. 2
   其他remained below 10° C
3. 3
   workup.ADDITIONwas added
4. 4
   温度to warm to room temperature
5. 5
   workup.STIRRINGstirring
6. 6
   workup.WAITwas continued for 17 h
7. 7
   过滤The reaction mixture was filtered through a pad of Celite® (50 g)
8. 8
   洗涤washed with additional methylene chloride
9. 9
   浓缩The filtrate was concentrated under reduced pressure
10. 10
    其他purified by silica gel column chromatography
11. 11
    洗涤eluting with methylene chloride

实验过程

Imidazole (26.6 g, 0.39 mol) was dissolved in methylene chloride (400 mL) at room temperature. Iodine (102.5 g, 0.39 mol) was added and the reaction mixture was stirred for 10 min at room temperature and then cooled to 0° C. Triphenylphosphine (102.5 g, 0.39 mol) was added portionwise over 10 min such that the internal temperature remained below 10° C. A solution of tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate (60.4 g, 0.31 mol) in methylene chloride (100 mL) was added dropwise. On completion of addition of tert-butyl (2R)-2-fluoro-3-hydroxypropylcarbamate, additional methylene chloride (200 mL) was added. The reaction mixture was allowed to warm to room temperature and stirring was continued for 17 h. The reaction mixture was filtered through a pad of Celite® (50 g) and washed with additional methylene chloride. The filtrate was concentrated under reduced pressure and purified by silica gel column chromatography eluting with methylene chloride. This procedure afforded tert-butyl (2R)-2-fluoro-3-iodopropylcarbamate as a white solid (64.7 g, 68%).

来源