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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535235생성일: 2026년 10월 25일

Carbon Tetrachloride → 9-Bromo-10-phenyl-anthracene

https://huagongshe.com/reaction/535235

반응식

참여 물질

역할이름HCID투입량
반응물Carbon TetrachlorideHCID 5943—
반응물9-PhenylanthraceneHCID 11766—
반응물BromineHCID 24408—
반응물Sodium ThiosulfateHCID 24477—
용매MethanolHCID 887—
생성물9-Bromo-10-phenyl-anthraceneHCID 4155836—

반응 단계

In a 300 mL three-neck flask, 5.8 g (23 mmol) of 9-phenylanthracene and 100 mL of carbon tetrachloride were placed. Then, 30 mL of a carbon tetrachloride solution containing 4.0 g (25 mmol) of bromine was dripped into the mixture under nitrogen stream. After dripping, the solution was stirred for 12 hours at room temperature. After a certain period, 100 mL of a 1.0 M sodium thiosulfate solution was added and stirred for 1 hour, and an aqueous layer of the mixture was extracted with chloroform. The obtained extracted solution and the organic layer were combined and washed with a 0.10 M sodium thiosulfate solution, a saturated aqueous solution of sodium hydrogen carbonate, and saturated saline in this order, and then, the organic layer was dried with magnesium sulfate. The mixture was gravity filtered, and the obtained filtrate was condensed to give a solid. A toluene solution of the solid was subjected to suction filtration through Celite (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 531-16855), Florisil (produced by Wako Pure Chemical Industries, Ltd., Catalog No. 540-00135), and alumina, and the filtrate was condensed to give a solid. Methanol was added to the solid, and this suspension was irradiated with ultrasonic waves. Then, 6.4 g of a solid substance, which was target pale yellow powder, was obtained by suction filtration in a yield of 84%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859108B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-bf035b40aaba4cc38bb7e5d6d9711d46
출처 메모uspto-grants-2014_10