関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Dimethyl methylphosphonate | HCID 12958 | — |
| 反応物 | Propionic acid, 3-ethylphenyl ester | HCID 2734115 | — |
| 反応物 | HCID 178506865 | HCID 178506865 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Dimethyl(2-oxo-4-phenylbutyl)phosphonate | HCID 2733973 | 89.7% |
反応手順
To a solution of 68 g of methyl-phosphonic-acid dimethyl ester (MW=124.8; 1.6 eq.) in 325 mL of THF was added 218 mL of n-hexyllithium (2.5M in hexane; 1.6 eq.) at −80° C. The mixture was stirred for 30 min and a solution of 60 g of ethyl-3-phenyl propionate (MW=178.23, d=1.01, 1.0 eq.) in 90 mL of THF was added. The mixture was allowed to warm to ambient temperature and 150 mL of water were added. After separation of the layers the organic layer was extracted twice with water. The pH value of the combined aqueous layers was adjusted to pH=2 with 5M HCl and then extracted twice with DCM. Removal of the organic solvents under reduced pressure gave 89 g of the title compound (Assay: 86.8%; Yield=89.7%). It is not necessary to dry to completion, a 50 w % solution in MED is also suitable for the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08481758B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-2d379244b2b54006aaa262f1dbcaf58b |
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| 出典メモ | uspto-grants-2013_07 |
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