98232-51-0

基本信息
8-甲氧基-3,4-二氫苯并[B]噁庚英-5(2H)-酮
8-甲氧基-3,4-二氫苯并[B]氧雜環(huán)庚-5(2H)-酮
8-methoxy-3,4-dihydrobenzo[b]oxepin-5(2H)-one
1-Benzoxepin-5(2H)-one, 3,4-dihydro-8-methoxy-
物理化學性質(zhì)
制備方法

41214-27-1
![8-甲氧基-3,4-二氫苯并[B]氧雜-5(2H)-酮](/CAS/GIF/98232-51-0.gif)
98232-51-0
以3-甲氧基苯氧基丁酸為原料合成8-甲氧基-3,4-二氫苯并[b]氧雜環(huán)庚-5(2H)-酮的一般步驟:在80℃條件下,將多聚磷酸(PPA)的氯苯溶液緩慢加入化合物Int-19d(22g,0.1mol)中,保持反應混合物在80℃下持續(xù)攪拌約15小時。反應完成后,移除溶劑,將殘余物溶解于乙酸乙酯中,依次用1N氫氧化鈉水溶液和飽和食鹽水洗滌。有機層經(jīng)無水硫酸鈉干燥,過濾后減壓濃縮,得到目標化合物Int-19e(14g,收率73%)。產(chǎn)物經(jīng)1H NMR(CDCl3)表征,化學位移δ:7.74(d,J = 8Hz,1H),6.63(d,J = 8Hz,1H),6.53(s,1H),4.21(t,J = 12Hz,2H),3.80(s,3H),2.84(t,J = 16Hz,2H),2.18-2.15(m,2H)。
參考文獻:
[1] Patent: WO2012/50848, 2012, A1. Location in patent: Page/Page column 109-110
[2] Bioorganic and Medicinal Chemistry, 2003, vol. 11, # 23, p. 5025 - 5033
[3] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 21, p. 9554 - 9573
[4] Justus Liebigs Annalen der Chemie, 1954, vol. 587, p. 38,47
[5] Synthetic Communications, 2009, vol. 39, # 15, p. 2664 - 2673