돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1476684생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1476684

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물1-Chloro-4-iodobenzeneHCID 12510—
반응물Sodium AzideHCID 33557—
반응물L-ProlineHCID 145742—
반응물2-EthynylthiopheneHCID 5246258—
반응물Sodium AscorbateHCID 23667548—
용매(Methanesulfinyl)methane--water (1/1)HCID 23503278—
생성물1-(4-chloro-phenyl)-4-(thiophen-2-yl)-1H-1,2,3-triazoleHCID 863036565.5%

반응 조건

온도65 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09402397B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-76a6409c3fb74f2d883e987204d32a0e
출처 메모uspto-grants-2016_08