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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2426022생성일: 2026년 10월 26일

5-Chloro-2,3-dimethoxybenzaldehyde → 1-(5-Chloro-2,3-dimethoxyphenyl)ethanol

https://huagongshe.com/reaction/2426022

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참여 물질

역할이름HCID투입량
반응물5-Chloro-2,3-dimethoxybenzaldehydeHCID 4172275—
반응물HCID 178418573HCID 178418573—
용매Diethyl EtherHCID 3283—
생성물1-(5-Chloro-2,3-dimethoxyphenyl)ethanolHCID 1409291575%

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온도0 °C

반응 단계

To a stirred solution of 5-chloro-2,3-dimethoxy-benzaldehyde (7.0 g, 34.90 mmol) in dry diethyl ether (500 mL) at 0° C. was added methylmagnesium bromide of 3.0 M in diethyl ether (29 mL, 87.22 mmol). The reaction mixture was brought to room temperature and stirred for 30 min; refluxed for 3 h; then cooled to 0° C. and quenched by adding saturated aqueous NH4Cl. The two liquid layers were separated. The aqueous layer was extracted with diethyl ether. The combined organic layers were washed with water, dried, and concentrated to the crude compound which was purified by silica gel column (10-25% ethyl acetate in hexanes) to afford 1-(5-chloro-2,3-dimethoxy-phenyl)-ethanol (5.67 g, 75%): 1H NMR (400 MHz, CDCl3): δ 7.00 (d, 1H), 6.81 (d, 1H), 5.11 (m, 1H), 3.86 (s, 6H), 2.30 (d, 1H), 1.48 (d, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07968538B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-7a1a98b2b4334265be402c99c68aeb87
출처 메모uspto-grants-2011_06