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HRID 2095974作成日:2026年10月27日

alpha-Hydroxyacetophenone → Cinnamoylbenzene

https://huagongshe.com/reaction/2095974

反応式

関与物質

役割名称HCID仕込み量
反応物alpha-HydroxyacetophenoneHCID 68490—
反応物6-(Pyrrolidin-1-yl)pyridine-3-carbaldehydeHCID 2794775—
反応物HCID 178418582HCID 178418582—
溶媒TetrahydrofuranHCID 8028—
生成物CinnamoylbenzeneHCID 718965%

反応手順

1.85 g (13.6 mmol) of 2-hydroxyacetophenone, 2.0 g of 6-(pyrrolidin-1-yl)nicotinaldehyde (1.34 mmol), and 10 ml of 25% NaOCH3 were reacted in 50 ml of dry THF to give 2.2 g (65%) of chalcone after purification. 1H NMR (300 MHz, CDCl3): δ 13.13 (bs, 1H), 8.34 (d, J=2.4 Hz, 1H), 7.85 (d, J=15.3 Hz, 1H), 7.84 (d, J=1.5 Hz, 1H), 7.74 (d, d, J=2.4, 9.0 Hz, 1H), 7.43 (d, d, d, J=1.5, 7.2, 8.4 Hz, 1H), 7.37 (d, J=15.3 Hz, 1H), 6.98 (d, d, J=0.9, 8.4 Hz, 1H), 6.89 (d, d, d, J=0.9, 7.2, 8.1 Hz, 1H), 6.37 (d, J=9.0 Hz, 1H), 3.49 (bs, 4H), 2.05-1.96 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08449936B2
出典データセットuspto-grants-2013_05
ORD IDord-d452afd942964a1eb4c45fb9630cbedf
出典メモuspto-grants-2013_05