二氟溴乙酸乙酯
化合物
二氟溴乙酸乙酯是一種有機化合物,化學式為C4H5BrF2O2。它可以二氟溴乙酸為原料,轉化為酰氯後和乙醇反應製得。[3]它和氫氧化鈉在甲醇溶液中反應,可以得到二氟溴乙酸鈉。[4]在三乙胺存在下,它和苄胺在乙酸乙酯中回流反應,可以得到N-苄基二氟溴乙酰胺。[5]
二氟溴乙酸乙酯 | |
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IUPAC名 Ethyl 2-bromo-2,2-difluoroacetate | |
別名 | Difluorobromoacetic acid ethyl ester |
識別 | |
CAS號 | 667-27-6 |
PubChem | 69585 |
ChemSpider | 62789 |
SMILES |
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InChI |
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EINECS | 211-567-0 |
性質 | |
化學式 | C4H5BrF2O2 |
摩爾質量 | 202.98 g·mol−1 |
外觀 | 無色液體 |
密度 | 1.583 g·cm−3(25 °C)[1] |
沸點 | 111—113 °C(384—386 K)[2] |
蒸氣壓 | 1.36 mmHg(25°C) |
危險性 | |
GHS危險性符號 | |
GHS提示詞 | 危險 |
H-術語 | H225, H314 |
P-術語 | P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
編輯- ^ H. Cohn, Ernst D. Bergmann. The Autoxidation of 1,1-Dibromo-2,2-Difluoroethylene and Tribromoethylene. Preparation of Dibromofluoro- and Fluorodibromo-Acetic Acid. Israel Journal of Chemistry. 1964, 2 (6): 355–361 [2021-11-09]. doi:10.1002/ijch.196400068. (原始內容存檔於2021-11-09) (英語). (頁面存檔備份,存於互聯網檔案館)
- ^ Knunyants, I. L.; Mukhametshin, F. M.; German, L. S.; Delyagina, N. I.; Korovushkin, G. G. Nucleophilic substitution in ethyl difluoro[(fluorosulfonyl)oxy]acetate. Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, 1985. 6: 1435-1437. ISSN 0002-3353
- ^ Jin Yang, Bin Sun, Hao Ding, Pan-Yi Huang, Xiao-Li Tang, Rong-Cheng Shi, Zhi-Yang Yan, Chuan-Ming Yu, Can Jin. Photo-triggered self-catalyzed fluoroalkylation/cyclization of unactivated alkenes: synthesis of quinazolinones containing the CF 2 R group. Green Chemistry. 2021, 23 (1): 575–581 [2021-11-09]. ISSN 1463-9262. doi:10.1039/D0GC03761C (英語).
- ^ Depei Meng, Lingchun Li, Adam Brown, Jean-Nicolas Desrosiers, Shengquan Duan, Cheryl M. Hayward, Zhengbiao He, Jinbo Hu, Teresa Makowski, Mark Maloney, Sébastien Monfette, Hahdi Perfect, Jared L. Piper, Min Zhou, Daniel W. Widlicka. A radical chlorodifluoromethylation protocol for late-stage difluoromethylation and its application to an oncology candidate. Cell Reports Physical Science. 2021-04, 2 (4): 100394 [2021-11-09]. doi:10.1016/j.xcrp.2021.100394 (英語).
- ^ Tamara Meiresonne, Guido Verniest, Norbert De Kimpe, Sven Mangelinckx. Synthesis of 2-Fluoro-1,4-benzoxazines and 2-Fluoro-1,4-benzoxazepin-5-ones by Exploring the Nucleophilic Vinylic Substitution (S N V) Reaction of gem -Difluoroenamides. The Journal of Organic Chemistry. 2015-05-15, 80 (10): 5111–5124 [2021-11-09]. ISSN 0022-3263. doi:10.1021/acs.joc.5b00507 (英語).