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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33079생성일: 2026년 10월 23일

Ethyl benzoylacetate → HCID 178487676, 화합물

https://huagongshe.com/ko/reaction/33079

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl benzoylacetateHCID 7170—
반응물3-MethoxyanilineHCID 10824—
반응물1,4-Dioxane hydrochlorideHCID 20443148—
반응물L-Ascorbic AcidHCID 54670067—
용매TolueneHCID 1140—
생성물HCID 178487676HCID 178487676—

반응 조건

온도280 °C

반응 단계

A solution of ethyl benzoylacetate (b) (100.0 g, 0.52 mol), m-anisidine (a) (128.1 g, 1.04 mol) and 4 N HCl/dioxane (5.2 mL) in toluene (1.0 L) was refluxed for 6.25 h in a Dean-Stark apparatus. The cooled toluene solution was successively washed with aqueous 10% HCl (2×300 mL), 1 N NaOH (2×300 mL), H2O (300 mL) and brine (150 mL). The toluene phase was dried (MgSO4), filtered and concentrated under reduced pressure to give a 1.2:1.0 mixture of ester c and amide d (144.6 g, 45%/38% crude yield) as a dark brown oil. The crude oil was heated to 280° C. for 80 min while distilling generated EtOH. The cooled dark solid obtained was triturated with CH2Cl2 (200 mL). The suspension was filtered and the resulting solid washed with CH2Cl2 to give e (22.6 g, 17% from a) as a beige solid: 1H NMR (DMSO-d6) δ 8.00 (d, J=9.0 Hz, 1H), 7.81-7.82 (m, 2H), 7.57-7.59 (m, 3H), 7.20 (d, J=2.2 Hz, 1H), 6.94 (dd, J=9.0, 2.2 Hz, 1H), 6.26 (s, 1H), 3.87 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE040525E1
출처 데이터셋uspto-grants-2008_09
ORD IDord-14a51161b171474ab725977e128c4cea
출처 메모uspto-grants-2008_09