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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79504생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/79504

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; emulsion) and neutralized with the addition of 1M HCl solution. The aqueous layer was extracted with ethyl acetate (3×), and the organics were combined. The organic layer was washed with water (2×), brine (1×), separated, dried over MgSO4, filtered, and concentrated in vacuo to afford the crude product as an oil. The residue was loaded onto a large fritted 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 an oil (39.4 g, 92%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841304B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f355148a131e46a1adb6b871665d0c23
출처 메모uspto-grants-2014_09