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HRID 646547作成日:2026年10月25日

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

https://huagongshe.com/reaction/646547

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) 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 mol) 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%). 1HNMR, 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705108B2
出典データセットuspto-grants-2010_04
ORD IDord-92461f754d3342429b4476462409b9fd
出典メモuspto-grants-2010_04