125982-23-2

基本信息
(S)-tert-Butyl (6-oxotetrahydro-2H-pyran-3-yl)carbamate
tert-butyl (S)-(6-oxotetrahydro-2H-pyran-3-yl)carbamate
Carbamic acid, N-[(3S)-tetrahydro-6-oxo-2H-pyran-3-yl]-, 1,1-dimethylethyl ester
制備方法

126587-35-7

125982-23-2
以(S)-4-((叔丁氧羰基)氨基)-5-羥基戊酸甲酯(25g,0.1mol,1.0當(dāng)量)為原料,將其溶解于甲苯(300mL)和乙酸(150mL)的混合溶劑中,加熱回流反應(yīng)5小時(shí)。反應(yīng)完成后,將反應(yīng)液冷卻至室溫,隨后在減壓條件下濃縮除去溶劑。將濃縮后的殘余物置于冰浴中,緩慢加入飽和碳酸氫鈉溶液調(diào)節(jié)pH至7-8。用乙酸乙酯對(duì)水相進(jìn)行三次萃取,合并有機(jī)相,用飽和食鹽水洗滌,無(wú)水硫酸鈉干燥。過(guò)濾后,將濾液濃縮,得到粗產(chǎn)物。粗產(chǎn)物通過(guò)乙酸乙酯和石油醚混合溶劑重結(jié)晶純化,得到目標(biāo)產(chǎn)物(S)-(6-氧代四氫-2H-吡喃-3-基)氨基甲酸叔丁酯(8.0g,收率37.2%),為白色粉末。產(chǎn)物經(jīng)GC-MS分析,分子離子峰為215。
參考文獻(xiàn):
[1] Tetrahedron Letters, 1989, vol. 30, # 29, p. 3803 - 3804
[2] Journal of Organic Chemistry, 1991, vol. 56, # 13, p. 4167 - 4176
[3] Patent: WO2018/67422, 2018, A1. Location in patent: Page/Page column 47; 48
[4] Patent: WO2015/168246, 2015, A1. Location in patent: Page/Page column 64; 75