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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1721생성일: 2026년 10월 23일

Triethylamine → HCID 178418448, 화합물

https://huagongshe.com/ko/reaction/1721

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물p-Toluenesulfonyl azideHCID 13661—
반응물7-(Benzyloxy)-4-hydroxy-2H-1-benzopyran-2-oneHCID 54708442—
용매TetrahydrofuranHCID 8028—
생성물HCID 178418448HCID 17841844890%

반응 단계

A solution of 7-benzyloxy -4-hydroxy coumarin (2.5 g, 9.3 mmol; prepared in accordance with Example 5) in anhydrous THF (40 mL) was mixed with triethylamine (0.9 g, 9 mmol) taken in a 100 mL 3-neck round-bottom flask under an atmosphere of N2. A solution of p-toluenesulfonyl azide (2.8 g, 14 mmol) in dry THF (20 mL) was added dropwise through an addition funnel. The mixture was stirred at room temperature for 3 hrs. The color of the solution turned orange. The solvent was rotary evaporated and the product was taken in CH2Cl2 and washed with water (3 times). Petroleum ether (twice the volume) was added to the solution and the solid precipitate was filtered with a flit and dried at 45° C. The product was recrystallized using CH2Cl2 ; yield 90%. The product was characterized by NMR: 13C NMR (100 MHz, CD2 Cl2): 173.3, 165.4, 158.7, 156.0, 136.0, 129.1, 128.8, 128.0, 127.6, 113.9, 113.0, 103.0, 75.7, 71.2; DSC--m. pt. 191° C. followed by decomposition; IR (KBr): 2182, 2154, 1717, 1647, 1605 cm-1 ; MS(APCI): (M+H), 295 (base peak).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726295
출처 데이터셋uspto-grants-1998_03
ORD IDord-eafe799634bf413884245083d524cea5
출처 메모uspto-grants-1998_03