반응 #3160
ord-bcf47efb084b407da3df0c21bd581e1b
반응 방정식
반응 조건
후처리
- 1기타nitrogen atmosphere on a dry ice-acetone bath at an inner temperature of -70° to -68° C., followed
- 2workup.STIRRINGby stirring for 50 minutes at the same temperature
- 3workup.STIRRINGby stirring for minutes at the same temperature
- 4기타Thereafter, the cooling bath was removed
- 5workup.ADDITIONfollowed by gradual addition of 9.5 ml of 10%-hydrochloric acid
- 6기타After the reaction
- 7추출subjected to extraction with isopropyl ether
- 8세척by washing with water
- 9건조drying with mirabilite and distilling-off of the solvent
- 10기타to obtain a residue
- 11workup.WAITthe mixture was left
- 12기타to precipitate a crystal
- 13여과The crystal was recovered by filtration
실험 절차
Then, 2.00 g (6.43 mM) of b-bromo-2-octylcoumaran and 28 ml of dry THF were placed in a 100 ml-three-necked flask. To the mixture, 4.5 ml (7.20 mM) of a 1.6M solution of butyllithium in hexane was added dropwise under stirring and nitrogen atmosphere on a dry ice-acetone bath at an inner temperature of -70° to -68° C., followed by stirring for 50 minutes at the same temperature. To the resultant mixture a solution of 3.2 ml (13.9 mM) of triisopropylborate in 5.7 ml of dry THF was added dropwise in 10 minutes at an inner temperature of -73° to -68° C., followed by stirring for minutes at the same temperature. Thereafter, the cooling bath was removed and the inner temperature was increased to room temperature, followed by gradual addition of 9.5 ml of 10%-hydrochloric acid. After the reaction, the reaction mixture was poured into water and subjected to extraction with isopropyl ether, followed by washing with water, drying with mirabilite and distilling-off of the solvent to obtain a residue. To the residue, hexane was added and the mixture was left standing in a freezer to precipitate a crystal. The crystal was recovered by filtration to obtain 1.19 g of 2-octylcoumaran-5-boronic acid (Yield: 67.1%).