102229-10-7

基本信息
叔丁基二甲基硅氧基乙醇
叔丁基二甲基羥乙氧基硅烷
羥乙氧基叔丁基二甲基硅烷
2-(叔丁基二甲基硅氧基)乙醇
2-(叔丁基二甲基硅基氧)乙醇
2-(叔丁基二甲基硅烷氧基)乙醇
叔丁基二甲基羥乙氧基硅烷 25G
2-[(叔丁基二甲基硅基)氧基]乙醇
叔丁基二甲基硅氧基乙醇,依維莫司中間體側(cè)鏈
2-(tert-Butyldimethylsiloxy)ethanol
2-tert-Butyldimethylsilyloxyethanol
(TERT.-BUTYLDIMETHYLSILYLOXY)ETHANOL
2-((tert-ButyldiMethylsilyl)oxy)etanol-
2-(tert-ButyldiMethylsiloxy)ethyl alcohol
2-(tert-Butyl-dimethylsilanyloxy)-ethanol
2-[(tert-ButyldiMethylsilyl)oxy]-1-ethanol
2-[[tert-Butyl(dimethyl)silyl]oxy]ethan-1-ol
2-[[(1,1-DiMethylethyl)diMethylsilyl]oxy]ethanol
物理化學(xué)性質(zhì)
常見問題列表

107-21-1

18162-48-6

102229-10-7
向NaH(12.9g,0.322mol,60%分散于礦物油中)的無水THF(500mL)懸浮液中緩慢滴加乙二醇(20.0g,0.322mol)的無水THF(100mL)溶液。室溫下攪拌反應(yīng)混合物1小時后,加入叔丁基二甲基氯硅烷(TBSCl,48.59g,0.322mol),繼續(xù)在室溫下攪拌1小時。反應(yīng)完成后,用10%的K2CO3水溶液(100mL)淬滅反應(yīng),隨后用甲基叔丁基醚(MTBE,3×300mL)萃取。合并有機相,用無水Na2SO4干燥,過濾后減壓濃縮。粗產(chǎn)物通過硅膠柱色譜法純化,采用1%至33%乙酸乙酯的石油醚溶液進行梯度洗脫,得到2-((叔丁基二甲基甲硅烷基)氧基)乙醇(55.0g,收率96%),為無色油狀物。
參考文獻:
[1] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 7, p. 2375 - 2385
[2] Organic Letters, 2016, vol. 18, # 18, p. 4534 - 4537
[3] Patent: US2016/122318, 2016, A1. Location in patent: Paragraph 0181
[4] Patent: WO2017/24018, 2017, A1. Location in patent: Paragraph 00131
[5] Journal of Medicinal Chemistry, 2007, vol. 50, # 9, p. 2157 - 2165
報價日期 | 產(chǎn)品編號 | 產(chǎn)品名稱 | CAS號 | 包裝 | 價格 |
2025/05/22 | B5851 | 2-[[叔丁基(二甲基)硅基]氧基]乙醇 2-[[tert-Butyl(dimethyl)silyl]oxy]ethanol | 102229-10-7 | 25g | 180元 |
2025/05/22 | XW1022291072 | 叔丁基二甲基硅氧基乙醇 2-(tert-butyldimethylsilanyloxy)ethanol;2-[(tert-butyldimethylsilyl)oxy]ethanol;2-[(tert-butyldimethylsilyl)oxy]-1-ethanol;2-tert-butyldimethylsilyloxyethanol;2-[[(1,1-dimethylethyl)dimethylsilyl]oxy]ethanol | 102229-10-7 | 25G | 70元 |
2025/05/22 | B5851 | 2-[[叔丁基(二甲基)硅基]氧基]乙醇 2-[[tert-Butyl(dimethyl)silyl]oxy]ethanol | 102229-10-7 | 100g | 600元 |