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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7200생성일: 2026년 10월 24일

Acetic Anhydride → 4-((2-Methyl-5-oxo-4(5H)-oxazolylidene)methyl)benzonitrile

https://huagongshe.com/ko/reaction/7200

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물AcetylglycineHCID 10972—
반응물4-CyanobenzaldehydeHCID 66042—
반응물Sodium AcetateHCID 517045—
용매AcetoneHCID 180—
생성물4-((2-Methyl-5-oxo-4(5H)-oxazolylidene)methyl)benzonitrileHCID 367080—

반응 조건

온도50 °C

반응 단계

Acetone (80.0 l) was introduced into a mixture of 4-formylbenzonitrile (15.0 kg, 114.5 mol), N-acetylglycine (19.2 kg, 162.4 mol) and anhydrous sodium acetate (9.4 kg, 114.5 mol) followed by introduction, with stirring, of acetic anhydride (35.0 l, 370.5 mol). The reaction mixture was stirred under reflux for 1 h. The resulting thin yellow suspension was cooled to 50° C. and ice-water (200 l) was added as quickly as possible, with stirring and cooling. The mixture was stirred at 20° C. for another 1 h. To isolate the product, the yellow suspension was pressed onto a centrifuge and washed with deionized water (75 l), isopropanol (40 l) and methyl-tert-butylether (75 l). The product was dried under reduced pressure at 40° C. Yield 18.17 kg (85.7 mol, 75.2% of theory). M.p.: 192–193° C.; MS (DCl): m/z=213 [M+H+]; 1H-NMR (DMSO-d6): δ=2.42 (s, 3H), 7.30 (s, 1H), 7.96 (d, 2H), 8.33 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084250B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-6c3f31a14b3b47a1ba8904aea201e513
출처 메모uspto-grants-2006_08