참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl phosphite, (C2H5O)2(OH)P | HCID 12977 | — |
| 반응물 | Ethyl oxoacetate | HCID 70211 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Ethyl 2-(acetyloxy)-2-(diethyl phosphono)acetate | HCID 4131038 | 50.9% |
반응 단계
Ethyl 2-oxoacetate (50%) (74 g, 724.8 mmol, 1.0 eq.) was added dropwise with stirring at 0° C. to a solution of diethyl hydrogen phosphite (50 g, 362.1 mmol, 1.0 eq.) in toluene (100 mL), under nitrogen. Et3N (110 g, 1.1 mol, 3.0 eq.) was added dropwise with stirring at 0° C. The resulting solution was stirred for 1 hour at room temperature. To the mixture was added acetic anhydride (37 g, 362.4 mmol, 1.0 eq.) dropwise with stirring at 0° C. The resulting solution was stirred overnight at room temperature. The pH value of the solution was adjusted to 6 with 2N HCl. The resulting solution was extracted with DCM (3×150 mL) and the organic layers were combined, dried over Na2SO4, and concentrated under vacuum. The residue was loaded onto a silica gel column with EtOAc:hexanes (1:2˜1:5) to yield the title compound (52 g) as a light yellow liquid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08586536B2 |
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| 출처 데이터셋 | uspto-grants-2013_11 |
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| ORD ID | ord-08489840de5a43bc9cedf30a80b9b792 |
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| 출처 메모 | uspto-grants-2013_11 |
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