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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3064생성일: 2026년 10월 24일

Water → 2-Octylcoumaran-5-boronic acid

https://huagongshe.com/ko/reaction/3064

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Triisopropyl borateHCID 21531—
반응물b-Bromo-2-octylcoumaranHCID 18934310—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-Octylcoumaran-5-boronic acidHCID 1893432367.1%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733476
출처 데이터셋uspto-grants-1998_03
ORD IDord-bcf47efb084b407da3df0c21bd581e1b
출처 메모uspto-grants-1998_03