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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50660생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/50660

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Diethyl EtherHCID 3283—
반응물Sodium HydroxideHCID 14798—
반응물2-Amino-5-bromobenzoic acidHCID 79858—
반응물HCID 178418573HCID 178418573—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-(2-Amino-5-bromophenyl)propan-2-olHCID 1204227557%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713478B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-0d885dd01d0a42a5a95c070c2d642ca4
출처 메모uspto-grants-2004_03