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HRID 1811026作成日:2026年10月27日

Aniline → 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide

https://huagongshe.com/reaction/1811026

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物Thionyl ChlorideHCID 24386—
反応物3-Bromo-6-hydroxy-2-methylbenzoic acidHCID 11053451—
反応物HCID 178418385HCID 178418385—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物3-bromo-6-hydroxy-2-methyl-N-phenylbenzamideHCID 5937498868.4%

反応条件

温度150 °C

反応手順

Step 3 Thionyl chloride (0.111 mL, 1.524 mmol) was added to a solution of benzotriazole (594 mg, 4.99 mmol) in DCM (8 mL) at rt and the mixture was stirred for 30 min. A solution of 3-bromo-6-hydroxy-2-methylbenzoic acid (320 mg, 1.385 mmol) in THF (8.00 mL) was added and the mixture was stirred at rt for 2 hrs. The mixture was filtered and the solid was washed with DCM (3 mL). The filtrate was concentrated, and the residue was dissolved in aniline (2 g, 21.48 mmol) and heated in a sealed tube by microwave irradiation at 150° C. for 10 min. The mixture was diluted with EtOAc (100 mL) and washed with 2 M hydrochloric acid (20 mL), water (10 mL) and brine (10 mL), dried and concentrated. The residue was triturated with DCM (4 mL) to give the 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide as light-colored solid (290 mg, 68%). Mass spectrum m/z 306, 308 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08362065B2
出典データセットuspto-grants-2013_01
ORD IDord-fddee5f9c6364155b35cd980ff925283
出典メモuspto-grants-2013_01