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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1175101생성일: 2026년 10월 27일

1-Decyne → 3-Decanyl-6-dec-1-ynyldithieno[3,2-b:2',3'-d]thiophene

https://huagongshe.com/reaction/1175101

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참여 물질

역할이름HCID투입량
반응물1-DecyneHCID 12997—
반응물2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiopheneHCID 16103475—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418397HCID 178418397—
용매TriethylamineHCID 8471—
생성물3-Decanyl-6-dec-1-ynyldithieno[3,2-b:2',3'-d]thiopheneHCID 6692501593%

반응 조건

온도130 °C

반응 단계

2-bromo-3-decanyldithieno[3,2-b:2′,3′-d]thiophene (92)(4.16 g, 0.01 mol) was mixed with 1-decyne (3.6 g, 0.026 mol), tetrakis(triphenylphosphine)palladium (0.58 g, 0.5 mmol) and copper(I) iodide (0.19 g, 1.0 mmol) in triethylamine (80 mL). This mixture was bubbled with nitrogen for 5 minutes and then heated up to 130° C. under argon for 16 hours. Triethylamine was evaporated and hexane (150 mL) was added. This mixture was filtered to remove solid salts. The organic layer was washed with 1 M hydrochloric acid (50 mL) and brine (50 mL) then dried over MgSO4. The solvent was removed in vacuo, and the residue was purified by chromatography on silica gel eluting with hexane to yield the target compound (3.87 g, 93.0%). 1H NMR, solvent CD2Cl2. δ 7.36 (d, 1H), 7.30 (d, 1H), 2.82 (t, 2H), 2.49 (t, 2H), 1.63-1.27 (m, 28H), 0.88 (m, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07838623B2
출처 데이터셋uspto-grants-2010_11
ORD IDord-19d7fa4606f246688414790cf03f8782
출처 메모uspto-grants-2010_11