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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 496321생성일: 2026년 10월 25일

2,7-Dibromo-9-(bis-methylsulfanyl-methylene)fluorene → 2,7-Dibromo-9-(bisdodecyl-methylene)fluorene

https://huagongshe.com/reaction/496321

반응식

참여 물질

역할이름HCID투입량
반응물2,7-Dibromo-9-(bis-methylsulfanyl-methylene)fluoreneHCID 12151612—
반응물HCID 178443215HCID 178443215—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물2,7-Dibromo-9-(bisdodecyl-methylene)fluoreneHCID 1215161762%

반응 조건

온도2.5 °C

반응 단계

To a solution of 2,7-dibromo-9-(bis-methylsulfanyl-methylene)fluorene (4.28, 10 mmol) in dry THF (70 ml) at 0° C. under nitrogen, was added a solution of lithium tetrachlorocuprate (2 ml of a 0.1M solution in THF, 2 mol %). A solution of dodecylmagnesium bromide (22 ml of a 1.0M solution in diethyl ether, 0.022 mol) was added dropwise over 15 min. The reaction was stirred for 3 h at 0-5° C. before quenching with 5% NaOH (100 ml). The reaction was stirred for 10 min and then filtered through celite. The organic layer was separated and the aqueous layer further washed with ethyl acetate (100 ml). The combined organics were washed with brine (100 ml), dried (sodium sulfate), and concentrated under reduced pressure. The crude oil was further purified by filtration through a plug of silica (5 cm×5 cm) covered with a layer of basic alumina (1 cm×5 cm), eluting with petrol. After concentration the residue was recrystallized from isohexane to afford 4.2 of the product as white crystals (62%). Purity (HPLC>98%). 1H and 13C NMR spectra as expected.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06943275B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-585997a7c7cb49ca877631d8a8a335c1
출처 메모uspto-grants-2005_09