참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Acetylglycine | HCID 10972 | — |
| 반응물 | 4-Cyanobenzaldehyde | HCID 66042 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 4-((2-Methyl-5-oxo-4(5H)-oxazolylidene)methyl)benzonitrile | HCID 367080 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07084250B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-6c3f31a14b3b47a1ba8904aea201e513 |
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| 출처 메모 | uspto-grants-2006_08 |
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