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HRID 575003作成日:2026年10月24日

Sodium Carbonate → 4,7-Bis(3-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole

https://huagongshe.com/ja/reaction/575003

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物4,7-Dibromo-2,1,3-benzothiadiazoleHCID 626361—
反応物2-(3-Hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 16663552—
触媒HCID 178418397HCID 178418397—
生成物4,7-Bis(3-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazoleHCID 56590608—

反応条件

温度100 °C

反応手順

4,7-Dibromobenzo[c]-1,2,5-thiadiazole (1.00 g, 3.41 mmol) and 3-hexylthiophene-2-boronic acid pinacol ester (2.10 g, 7.14 mmol) were placed in a 100 mL 3-neck round bottom flask which was flushed with N2 gas for 5 minutes. Dimethoxyethane (20 mL) and water (30 mL) were added and the mixture was purged with N2 gas for 30 minutes. Sodium carbonate (4.23 g, 34.1 mmol) and catalyst Pd(PPh3)4 (0.430 g, 0.372 mmol) were added and the mixture was heated to 100° C. and stirred for 12 hours. The mixture was extracted into hexanes and passed through a silica column, by eluting first with hexanes (200 mL) and then eluting the product with a solution of 5% EtOAc in hexanes (200 mL). The procedure afforded 1.59 g of vibrant orange, 4,7-bis(3-hexylthiophen-2-yl)benzo[c][1,2,5]thiadiazole (Formula 2) in 99% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09035016B2
出典データセットuspto-grants-2015_05
ORD IDord-611fa25be5834b5f844f5d43c6edef8d
出典メモuspto-grants-2015_05