関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Ethyl phosphite, (C2H5O)2(OH)P | HCID 12977 | — |
| 反応物 | Ethyl oxoacetate | HCID 70211 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Ethyl 2-(acetyloxy)-2-(diethyl phosphono)acetate | HCID 4131038 | 50.9% |
反応手順
Ethyl 2-oxoacetate (50%) (74 g, 724.8 mmol) was added dropwise with stirring at 0° C. to a solution of diethyl hydrogen phosphite (50 g, 362.1 mmol) in toluene (100 mL), under nitrogen. Et3N (110 g, 1.1 mol) 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) 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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09150500B2 |
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| 出典データセット | uspto-grants-2015_10 |
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| ORD ID | ord-a2e3d7ab571a46a9be8ca07e8c1f3616 |
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| 出典メモ | uspto-grants-2015_10 |
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