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HRID 83968作成日:2026年10月26日

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

https://huagongshe.com/reaction/83968

反応式

関与物質

役割名称HCID仕込み量
反応物1-DecyneHCID 12997—
反応物2-Bromo-3-decanyldithieno[3,2-b:2',3'-d]thiopheneHCID 16103475—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
溶媒TriethylamineHCID 8471—
生成物3-Decanyl-6-dec-1-ynyldithieno[3,2-b:2',3'-d]thiopheneHCID 6692501593%

反応条件

温度130 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846855B2
出典データセットuspto-grants-2014_09
ORD IDord-9d2b35e796fd49cd9260fe781ff6458e
出典メモuspto-grants-2014_09