돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1185생성일: 2026년 10월 23일

Phloroglucinol → 5,7-Dihydroxy-4-propylcoumarin

https://huagongshe.com/ko/reaction/1185

반응식

참여 물질

역할이름HCID투입량
반응물PhloroglucinolHCID 359—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물Ethyl 3-oxohexanoateHCID 238498—
용매WaterHCID 962—
생성물5,7-Dihydroxy-4-propylcoumarinHCID 539126099.1%

반응 단계

A suspension of anhydrous phloroglucinol (20.0 g, 0.159 mol) in ethyl butrylacetate (26.3 g; 0.167 mol) was added over 30 min to 50 g of constantly stirred trifluoromethanesulfonic acid cooled in an ice bath. A drying tube was then fined to the reaction vessel and the mixture was stirred for 16h at 25° C., after which the resulting thick paste was combined with ice (200 g) and water (300 mL) with brisk stirring. After 30 min the solid material was collected by vacuum filtration and recrystallised from 95% ethanol to yield coumarin 15 (34.7 g; 99%) as lemon yellow crystals. mp 236°-238° C. 1H NMR (CDCl3 /CD3OD 3:1): δ6.13(1H, d; J =2.3 Hz), 6.04(1H, d; J=2.3 Hz), 5.68(1H, s), 2.76(2H, t; J=7.4 Hz), 1.47(2H, tq; J =7.7, 7.4 Hz), 0.82(3H, t; J =7.7 Hz). 13C NMR (CDCl3 /CD3OD 3:1): δ163.1, 160.7, 160.6, 157.3, 156.7, 107.8, 102.5, 99.2, 95.0, 37.7, 22.5, 13.4. Anal. calc. for C12H12O4.(H2O): C, 60.50; H, 5.92. Found: C, 60.47; H, 5.92.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723631
출처 데이터셋uspto-grants-1998_03
ORD IDord-66f1b1423ff84fd0aecb09103bf3af98
출처 메모uspto-grants-1998_03