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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2,7-Dibromo-9-(bis-methylsulfanyl-methylene)fluorene | HCID 12151612 | — |
| 반응물 | HCID 178443215 | HCID 178443215 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2,7-Dibromo-9-(bisdodecyl-methylene)fluorene | HCID 12151617 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06943275B2 |
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| 출처 데이터셋 | uspto-grants-2005_09 |
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| ORD ID | ord-585997a7c7cb49ca877631d8a8a335c1 |
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| 출처 메모 | uspto-grants-2005_09 |
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