123387-53-1
123387-53-1 結構式
基本信息
3,4-二氫喹啉-1(2H)-甲酸叔丁酯
3,4-二氫喹啉-1(2H)-羧酸叔丁酯
t-Butyl 3,4-dihydro-2H-quinoline-1-carboxylate
tert-butyl 3,4-dihydro-2H-quinoline-1-carboxylate
tert-Butyl 3,4-dihydroquinoline-1(2H)-carboxylate
tert-butyl 1,2,3,4-tetrahydroquinoline-1-carboxylate
1(2H)-Quinolinecarboxylic acid, 3,4-dihydro-, 1,1-dimethylethyl ester
物理化學性質(zhì)
制備方法
635-46-1
24424-99-5
123387-53-1
一般步驟:在氮氣保護下,將1,2,3,4-四氫喹啉(626 mg,4.7 mmol)溶于乙腈(15 mL)中,依次加入三乙胺(1.3 mL,9.3 mmol)和4-二甲氨基吡啶(DMAP,112 mg,0.19 mmol)。隨后,向反應體系中緩慢加入二碳酸二叔丁酯(1.181 g,5.4 mmol)。反應混合物在室溫下攪拌1.5小時后,升溫至55℃繼續(xù)反應過夜。反應完成后,將混合物冷卻至室溫,減壓濃縮除去溶劑。將殘余物用乙酸乙酯(25 mL)和1M鹽酸(25 mL)進行分配萃取。分離有機相,依次用1M鹽酸(2×25 mL)和飽和食鹽水(25 mL)洗滌。有機相經(jīng)無水硫酸鈉干燥后,過濾并減壓濃縮。粗產(chǎn)物通過硅膠快速柱色譜法純化(Combiflash系統(tǒng),洗脫梯度:0%至40%乙酸乙酯/己烷),得到3,4-二氫喹啉-1(2H)-甲酸叔丁酯(139 mg,收率13%)為無色油狀物。
參考文獻:
[1] Chemistry - A European Journal, 2016, vol. 22, # 36, p. 12891 - 12903
[2] Patent: WO2015/48553, 2015, A1. Location in patent: Page/Page column 15; 32
[3] Tetrahedron, 2015, vol. 71, # 29, p. 4738 - 4744
[4] Organic and Biomolecular Chemistry, 2018, vol. 16, # 11, p. 1971 - 1975
[5] Chemistry - A European Journal, 2018, vol. 24, # 32, p. 8051 - 8055