戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 416619作成日:2026年10月24日

Benzoyl chloride, 3-nitro- → HCID 178522383、化合物

https://huagongshe.com/ja/reaction/416619

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl chloride, 3-nitro-HCID 8495—
反応物Sodium CarbonateHCID 10340—
反応物3-Amino-4-hydroxypyridineHCID 233392—
溶媒PyridineHCID 1049—
生成物HCID 178522383HCID 17852238379.3%

反応手順

A solution of 3-nitrobenzoyl chloride (3.339 g, 18.0 mmol) in pyridine (54.0 mL) was added dropwise to a solution of 3-amino-4-hydroxypyridine (2.376 g, 21.6 mmol) in pyridine (36.0 mL) at 10° C. and the resultant mixture was stirred overnight. Na2CO3 (1.145 g, 10.8 mmol) was added and the mixture was stirred for 1 h. The solid was collected by filtration, washed with 10% HOAc (30 mL×3) and water (30 mL×3), and dried under vacuo to afford N-(4-hydroxypyridin-3-yl)-3-nitrobenzamide as yellow solid (3.70 g, yield: 66%). 1H-NMR (400 MHz, DMSO-dB6B) δ: 6.34 (1H, d, J=7.2 Hz), 7.74 (1H, d, J=8.0 Hz), 7.84 (1H, t, J=8.0 Hz), 8.34 (1H, d, J=7.2 Hz), 8.44 (1H, t, J=8.0 Hz), 8.66 (1H, s), 8.73 (1H, s), 9.66 (1H, s), 11.65 (1H, br s); MS (ESI) calcd. for C12H9N3O4 (m/z): 259. found: 260 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088928B2
出典データセットuspto-grants-2012_01
ORD IDord-f37d6ee0443641de97cbd16fba6b169a
出典メモuspto-grants-2012_01