참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethyl Sulfoxide | HCID 679 | — |
| 반응물 | 2-Propenoic acid, 3,3-diethoxy-, ethyl ester | HCID 169388 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Benzamidine HCl hydrate | HCID 16219042 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | 6-Ethoxy-2-phenylpyrimidin-4(3H)-one | HCID 608431 | 57% |
반응 단계
A mixture of 3.14 g (20.0 mmol) of benzamidine hydrochloride hydrate, 1.65 g (20.1 mmol) of powdered anhydrous sodium acetate, 4.17 g (22.2 mmol) of ethyl 3,3-diethoxyacrylate and 10 mL of DMSO was heated at 120° C. for 8 h. The mixture was cooled, diluted with 50 mL of 5% aqueous NaOH and washed with two 100 mL portions of ether. The aqueous layer was acidified with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum at 50° C. to furnish 2.28 g (57%) of crude 6-ethoxy-2-phenyl-4(3H)-pyrimidinone as a yellow solid 1 H-NMR (d6-DMSO) δ 1.35(3H,t), 4.33(2H,q), 5.60(1H,s), 7.50(3H,m), 8.2(2H,m).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05726124 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-2b0378d7412b4bedb3ed0ed2242b2a38 |
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| 출처 메모 | uspto-grants-1998_03 |
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