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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 83968생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/83968

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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) is 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 is bubbled with nitrogen for 5 minutes and then heated to 130° C. under argon for 16 hours. Triethylamine is evaporated and hexane (150 mL) is added. The mixture is filtered to remove solid salts and the organic layer is washed with 1M hydrochloric acid (50 mL) and brine (50 mL), then dried over MgSO4. The solvent is removed in vacuo, and the residue is purified by chromatography on silica gel eluting with hexane to yield the target compound (3.87 g, 93.0% yield). 1HNMR (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 번호US08846855B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-9d2b35e796fd49cd9260fe781ff6458e
출처 메모uspto-grants-2014_09