反応 #792189

反応方程式

NaN3

2-ethynylthiophene

1-chloro-4-iodobenzene

L-proline

Na2CO3

sodium ascorbate

→

1-(4-chloro-phenyl)-4-(thiophen-2-yl)-1H-1,2,3-triazole

収率 5.5%

溶媒

DMSO H2O

反応条件

後処理

1. 1
   その他the vessel was sealed
2. 2
   抽出extracted with ethyl acetate
3. 3
   その他The organic layer was separated
4. 4
   洗浄washed with brine
5. 5
   乾燥dried over Na2SO4
6. 6
   濃縮concentrated under vacuum
7. 7
   その他The crude product was then purified by silica column (100-200)

実験手順

A sealed tube was sequentially charged with 2-ethynylthiophene (250 mg, 2.31 mol), 1-chloro-4-iodobenzene (551 mg, 2.31 mmol, 1.0 eq.), L-proline (53 mg, 0.462 mmol, 0.2 eq.), Na2CO3 (50 mg, 0.462 mmol, 0.2 eq.), sodium ascorbate (91 mg, 0.462 mmol, 0.2 eq.), and 4 mL of DMSO:H2O (9:1). Then NaN3 (180 mg 2.77 mmol, 1.2 eq.) and CuSO4.5H2O (58 mg. 0.231 mmol, 0.1 eq.) were added, and the vessel was sealed. The suspension was stirred at 65° C. for 16 hours. The reaction mixture was then poured into ice-water and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried over Na2SO4, and concentrated under vacuum. The crude product was then purified by silica column (100-200) using 15-20% ethyl acetate/hexanes to yield 1-(4-chloro-phenyl)-4-(thiophen-2-yl)-1H-1,2,3-triazole as a brown solid compound (34 mg, 0.13 mmol yield 5.5%). LC-MS [M+H] 261.8 (C12H8ClN3S+H, expected 262.01). The 1H-NMR spectra was in accordance with the chemical structure.

出典