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HRID 50660作成日:2026年10月27日

Hydrochloric Acid → 2-(2-Amino-5-bromophenyl)propan-2-ol

https://huagongshe.com/reaction/50660

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Diethyl EtherHCID 3283—
反応物Sodium HydroxideHCID 14798—
反応物2-Amino-5-bromobenzoic acidHCID 79858—
反応物HCID 178418573HCID 178418573—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物2-(2-Amino-5-bromophenyl)propan-2-olHCID 1204227557%

反応手順

A solution of 2-amino-5-bromobenzoic acid (10 g, 46 mmol) in dry THF (200 mL) was treated at −78° C. under nitrogen with a solution of methylmagnesium bromide in ether (3.0 M, 90 mL, 270 mmol). The reaction mixture was slowly warmed to ambient temperature, kept stirring for 48 hours under nitrogen and then poured into a cold 0.5 N aqueous hydrochloride solution (300 mL). The mixture was neutralized with aqueous 1 N sodium hydroxide solution and ethyl acetate (300 mL) was added. The organic layer was separated and aqueous layer was extracted with ethyl acetate (3×100 mL). The combined organic layers were washed with brine and dried (MgSO4). After removal of solvent in vacuo, the residue was purified by a silica gel flash chromatography (hexane:ethyl acetate/3:2) to give 2-(2-amino-5-bromophenyl)propan-2-ol as off-white solid (6 g, 57%): mp 62-63° C.; 1H-NMR (CDCl3) δ 7.19 (d, 1H, J=2.3 Hz), 7.12 (dd, 1H, J=8.4, 2.3 Hz), 6.51 (d, 1H, J=8.4 Hz), 4.70 (s, 2H), 1.82 (s, 1H), 1.65 (s, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713478B2
出典データセットuspto-grants-2004_03
ORD IDord-0d885dd01d0a42a5a95c070c2d642ca4
出典メモuspto-grants-2004_03