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HRID 564495作成日:2026年10月25日

Hydrochloric Acid → (3-Bromo-4-methoxyphenyl)methanamine

https://huagongshe.com/reaction/564495

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物BoraneHCID 6331—
反応物TetrahydrofuranHCID 8028—
反応物3-Bromo-4-methoxybenzonitrileHCID 736049—
溶媒EthanolHCID 702—
生成物(3-Bromo-4-methoxyphenyl)methanamineHCID 22026276—

反応条件

温度50 °C

反応手順

3-Bromo-4-(methyloxy)benzonitrile (2.12 g, 10 mmol), THF (30 mL), and 1.5 M borane in THF (30 mL, 45 mmols) were combined and stirred under argon at reflux. The additional 1.5 M borane in THF (30 mL, 45 mmols) and reflux continued. THF (30 mL), and 1.5 M borane in THF (30 mL, 45 mmols) was again added and the mixture refluxed for a total of ten days to drive the reaction to completion. The reaction was worked up by the cautious addition of ethanol followed by 1N HCl until the pH was 2. This mixture was then heated to 50° C. for 4 h. The solvents were pumped off, and the residue partitioned between EtOAc and water. The aqueous phase was washed 3× with EtOAc and adjusted to pH 10 by the addition of 2.5 N NaOH. The aqueous phase was extracted 3× with EtOAc. The combined organic phases were dried over anhydrous Na2SO4, filtered and concentrated to give the title compound. LC-MS m/z 198.7 (M−NH2), 0.99 min (ret time).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08067408B2
出典データセットuspto-grants-2011_11
ORD IDord-49cc177301fa4a26926a7c90e5ac8efe
出典メモuspto-grants-2011_11