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HRID 63616作成日:2026年10月26日

Acetic Acid → 6-Bromo-3,4-dihydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/63616

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sulfuric AcidHCID 1118—
反応物Trimethylsilyl cyanideHCID 82115—
反応物6-Bromo-1-tetraloneHCID 10105069—
触媒zinc(II)iodideHCID 9883512—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物6-Bromo-3,4-dihydronaphthalene-1-carboxamideHCID 11859834380%

反応条件

温度60 °C

反応手順

To a solution of 6-bromo-1,2,3,4-tetrahydronaphthalen-1-one (5.46 g, 24.3 mmol) and ZnI2 (50 mg) in toluene (50 mL) was added TMSCN (4.82 mL, 48.6 mmol), and the solution stirred at 60° C. overnight. The reaction was cooled to rt, and H2SO4 (5.6 mL) was added. Then AcOH (34 mL), H2SO4 (25 mL) and H2O (4 mL) were added to the reaction, and it was heated to 105° C. for 3 h. The mixture was cooled and poured over ice-water (250 mL). The precipitate was collected by filtration, washed with water, and dried under vacuum to give 4.88 g (80%) of the title compound as an off-white solid. 1H NMR (400 MHz, DMSO-d6): δ 2.25-2.33 (2H, m), 2.72 (2H, t, J=8.0 Hz), 6.51 (1H, t, J=4.6 Hz), 7.20 (1H, br s), 7.35-7.40 (3H, m), 7.65 (1H, br s). [M+H] calc'd for C11H10BrNO, 252, 254. found 252, 254.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447046B2
出典データセットuspto-grants-2016_09
ORD IDord-6bb6bfdcada2480cbbd54a1d34aaccd8
出典メモuspto-grants-2016_09