돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1356493생성일: 2026년 10월 26일

Formic Acid → Azithromycin

https://huagongshe.com/reaction/1356493

반응식

참여 물질

역할이름HCID투입량
반응물Formic AcidHCID 284—
반응물FormaldehydeHCID 712—
반응물WaterHCID 962—
반응물9-Deoxo-9a-aza-9a-homoerythromycin AHCID 9810601—
용매AcetoneHCID 180—
생성물AzithromycinHCID 44704377%

반응 조건

온도58 °C

반응 단계

In a 0.25 L three-necked round bottom flask equipped with a mechanical stirrer, a condenser and thermometer, 25 g of desmethyl-azithromycin was dissolved in 102 mL of acetone. Formaldehyde (5.3 mL) and formic acid (2.6 mL) were added and the clear solution was heated to reflux (˜58° C.). The mixture was maintained under reflux for 3 hours then cooled to less than 40° C. and 102 mL of water was added. The acetone was separated from the reaction mixture by distillation under low vacuum (˜300 mbar). The distillation was stopped when the temperature of the liquid phase reaches ˜40° C./300 mbar. Activated carbon SXI (1.25 g) was added and the suspension was mixed for 1 hour. Then the activated carbon was separated from the solution by filtration on a Büchner filter containing Hyflow. The filter cake was washed with 102 mL of water. The pH was adjusted with an NaOH solution of 47% to 10-10.5 (˜3.14 g). A massive precipitation of Azithromycin was observed. After stirring the suspension for 1 hour, the crude azithromycin was separated by filtration, washed twice with 25 mL of water and dried at 40° C. in a vacuum oven for>24 hours. After drying, 19.7 g of crude azithromycin was obtained (yield 77% based on weight). No impurities that were derivatives of azithromycin were detected.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06586576B2
출처 데이터셋uspto-grants-2003_07
ORD IDord-b1980129035f49fcba93284598f2af6a
출처 메모uspto-grants-2003_07