Английская Википедия:3-Hydroxytetrahydrofuran
3-Hydroxytetrahydrofuran (3-OH THF) is a colorless liquid with a normal boiling point of 179 °C[1] and boiling at 88−89 °C at 17 mmHg,[2] with density (1.087 g/cm3 at 19 °C).[3] 3-OH THF is a useful pharmaceutical intermediate. The enantiopure (absolute configuration S) version of this compound is an intermediate to launched retroviral drugs.[4]
Synthesis
3-Hydroxytetrahydrofuran was prepared in 1910 by Pariselle[5] via cyclization and hydrolysis of 3,4-Dibromo-1-methoxybutane. Chiral 3-hydroxytetrahydrofuran (both (S) – and (R)-forms) has been synthesized in high enantiomeric purity from (S)- and (R)-1,2,4-butanetriol, respectively, obtained from chiral feedstocks. Thus, the chiral (S)-1,2,4-butanetriol intermediate was cyclized to chiral (S)-3-hydroxytetrahydrofuran in the presence of p-toluenesulfonic acid (PTSA) catalyst at temperatures of 180−220 °C.[6] Similarly, (S)-3-hydroxytetrahydrofuran was prepared in 95.8% optical purity from L-malic acid via an esterification-reduction-cyclodehydration sequence.[7] 3-hydroxytetrahydrofuran has been synthesized via hydroboration of 2,3- and 2,5-dihydrofuran employing various borane reagents[8] and chiral 3-hydroxytetrahydrofurans have also been prepared by catalytic asymmetric hydroboration of 2,3- and 2,5-dihydrofurans with a borane in the presence of a homogeneous chiral platinum complex, followed by oxidation.[9] Racemic 3-hydroxytetrahydrofuran may be prepared in analogous fashion from racemic butanetriol, employing PTSA catalyst for the dehydrocyclization. Alternatively, 1,2,4-butanetriol may be converted to 3-hydroxytetrahydrofuran by treating with ethylene carbonate, followed by pyrolysis of the resulting carbonate ester.[10]
Applications
3-Hydroxytetrahydrofuran is an intermediate to the AIDS drugs amprenavir and fosamprenavir.[4] Additionally, 3-OH THF has been an intermediate to developmental drug substances, such as chemotherapy agents. For example, reaction of phosphorus pentasulfide with 3-hydroxytetrahydrofuran has been used in the synthesis of bis(O,O-di(tetrahydrofuran-3-yl)hydrogen dithiophosphate)platinum(II), a cisplatin analog.[11] 3-hydroxytetrahydrofuran may be converted into a range of tetrahydrofuran derivatives, many of which also serve as intermediates to compounds of pharmaceutical interest. For example, tetrahydrofuran-3-one (3-ketotetrahydrofuran)[12] and 3-aminotetrahydrofuran[13] have been synthesized from 3-hydroxytetrahydrofuran and used in pharmaceutical syntheses. Additionally, additive amounts (0.05-0.15 weight %) of the nitrate ester manufactured by sulfuric acid-nitric acid nitration of 3-hydoxytetrahydrofuran have been found to increase the quality (cetane number) of diesel fuel.[14]
References
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ 4,0 4,1 Venkata Mandava, et al., "Preparation of fosamprenavir calcium" U.S. Pat. Appl., 20110224443 (2011)
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Шаблон:Cite journal
- ↑ Anita Schnyder, et al., "Preparation of optically active 3-hydroxytetrahydrofurans by catalytic asymmetric hydroboration of dihydrofurans" Ger. Offen., 19807330 (1998)
- ↑ Шаблон:Cite journal
- ↑ Anthony Lowe, et al., "Dithiophosphato platinum complexes for the treatment of cancers" PCT Int. Appl., 2005095425 (2005)
- ↑ Шаблон:Cite journal
- ↑ Liren Jin, et al., "Process for preparation of (R)-3-aminotetrahydrofuran" Faming Zhuanli Shenqing Gongkai Shuomingshu, CN 1660829 A 20050831 (2005)
- ↑ Allen H. Filbey, "Diesel fuel composition" U.S. Pat., 4406665 (1983)
