Alcoholysis of fluoroform

作者：Miloserdov Fedor M; Grushin Vladimir V^*

来源：Journal of Fluorine Chemistry, 2014, 167: 105-109.

DOI：10.1016/j.jfluchem.2014.06.006

• Fluoroform
• CHF3
• HFC-23
• Alcoholysis
• Orthoformates

Fluoroform (CHF3) reacts with alkali metal alkoxides MOR (M = Na, K) in the corresponding alcohols ROH (R = Me, Et, i-Pr, t-Bu, and Allyl) at 80-120 degrees C to give orthoformate esters HC(OR)(3) in 55-90% yield. Particularly notable is the formation of HC(OBu-t)(3) in 75-80% yield (62% isolated yield; X-ray), an exotic organic compound that has been previously synthesized only once (3% yield). Solutions of NaOH in ROH (R = Me, Et, i-Pr and t-Bu) react with CHF3 to give NaF, HCOONa, and orthoformates HC(OR)(3). Hydrolysis of fluoroform with MOH (M = Na, K) at 140 degrees C produces largely MF and HCOOM along with small quantities of CO.

• 出版日期2014-11