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HRID 428343作成日:2026年10月25日

Tributylamine → N,N-Diisopropyl-3-(2-thienyl)propenamide

https://huagongshe.com/reaction/428343

反応式

関与物質

役割名称HCID仕込み量
反応物TributylamineHCID 7622—
反応物2-BromothiopheneHCID 13851—
反応物Tri-o-tolylphosphineHCID 80271—
反応物N,N-DiisopropylacrylamideHCID 559397—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒DimethylformamideHCID 6228—
生成物N,N-Diisopropyl-3-(2-thienyl)propenamideHCID 4444087—

反応条件

温度130 °C

反応手順

2-Bromothiophene (2.28 g, 14.0 mmol), N,N-diisopropylacrylamide (1.55 g, 10.0 mmol), palladium(II)acetate (34 mg, 0.15 mmol), tri-o-tolylphosphine (183 mg, 0.6 mmol), tri-n-butyl amine (2.04 g, 11.0 mmol) and dry DMF (5 mL) were mixed under a N2-atmosphere. The mixture was heated to 130° C. for 9 hours. Diethyl ether and H2O was added to the somewhat cooled mixture. The aqueous phase was extracted twice with diethyl ether. The combined organic phases were washed twice with 2 M HCl, once with water, once with brine, and dried (MgSO4), and the solvent was then evaporated. The crude product was chromatographed on silica (petroleum ether-ethyl acetate 4:1), affording a yellow oil, 1.58 g (66%): 1H NMR (CDCl3) 67 1.35 (br, 12H), 3.9 (br, 1H), 4.1 (br 1H), 6.65 (d, 1H), 7.00-7.30 (m, 3H), 7.72 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313132B1
出典データセットuspto-grants-2001_11
ORD IDord-bd6dd6ada6b640f69bd0ffc231d41bb5
出典メモuspto-grants-2001_11