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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82364생성일: 2026년 10월 24일

Hydrochloric Acid → Methyl 2-(4-chlorophenyl)-3-hydroxypropanoate

https://huagongshe.com/ko/reaction/82364

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물FormaldehydeHCID 712—
반응물Methyl 4-chlorophenylacetateHCID 104196—
촉매Sodium MethoxideHCID 10942334—
용매Dimethyl SulfoxideHCID 679—
생성물Methyl 2-(4-chlorophenyl)-3-hydroxypropanoateHCID 1991473392.2%

반응 단계

Methyl 2-(4-chlorophenyl)acetate (36.7 g, 199 mmol) and paraformaldehyde (6.27 g, 209 mmol) were dissolved/suspended in DMSO (400 mL) and treated with NaOMe (537 mg, 9.94 mmol). The mixture was allowed to stir at room temperature for 2 hours to completion by TLC analysis of the crude. The reaction was poured into ice-cold water (700 mL; white emulsion) and neutralized with the addition of 1M HCl solution. The aqueous portion was extracted with ethyl acetate (3×), and the organics were combined. The organic portion was washed with water twice, once with brine, separated, dried over MgSO4, filtered, and concentrated in vacuo to afford the crude product as a yellow oil. The residue was loaded onto a large fitted filtered with silica gel and eluted with 9:1 hexanes:ethyl acetate until the starting material/olefin were collected. The plug was then eluted with 1:1 hexanes:ethyl acetate until the pure desired product was eluted completely. The concentrated pure fractions yielded methyl 2-(4-chlorophenyl)-3-hydroxypropanoate as a colorless oil (39.4 g, 92%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846681B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3b794dbd2fff401d8ced19f2ec0b62d5
출처 메모uspto-grants-2014_09