反应详情

1-[1-Triphenylmethyl-5-imidazoyl]-3-(diethoxyphosphinyl)oxy-4-p-toluenesulfonyl-6-cyclohexyl-3-hexene (14.5 g, 0.018 mol) was dissolved in dry THF (150 ml) and HMPA (10 ml) at room temperature under N2. Sml2 (0.1M solution in THF) was added to the reaction in 50 ml portions via syringe. A total of 400 ml of 0.1M Sml2 was added. After the last 50 ml portion was added, the blue reaction mixture was stirred for 1 hour. The reaction mixture was added to 500 ml of a saturated solution of ammonium chloride and extracted with ethyl acetate (2×500 ml). The ethyl acetate layer was washed with brine (250 ml), water (2×400 ml) and brine (250 ml). The ethyl acetate layer was separated, dried over MgSO4, filtered and evaporated in vacuo to give a yellow oil. The crude acetylene was taken up in 25 ml of CHCl3 and filtered through a pad of silica gel (200 g) using 1 liter of ethyl acetate/hexanes (2:8). The filtrate was evaporated in vacuo to afford a viscous yellow oil which solidified upon standing. The solid was triturated with hexanes, filtered and washed with hexanes to give 5.5 g of 1- [1-triphenylmethyl-1H-imidazol-4-yl]-6-cyclohexyl-3-hexyne.

1. customat room temperature
2. additionA total of 400 ml of 0.1M Sml2 was added
3. additionAfter the last 50 ml portion was added
4. customthe blue reaction mixture
5. extractionextracted with ethyl acetate (2×500 ml)
6. washThe ethyl acetate layer was washed with brine (250 ml), water (2×400 ml) and brine (250 ml)
7. customThe ethyl acetate layer was separated
8. dry with materialdried over MgSO4
9. filtrationfiltered
10. customevaporated in vacuo
11. customto give a yellow oil
12. filtrationfiltered through a pad of silica gel (200 g)
13. customThe filtrate was evaporated in vacuo
14. customto afford a viscous yellow oil which
15. customThe solid was triturated with hexanes
16. filtrationfiltered
17. washwashed with hexanes