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Acetic Acid → Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Dimethyl methylphosphonate | HCID 12958 | — |
| 反応物 | Methyl 2-(3-chlorophenyl)acetate | HCID 2733544 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonate | HCID 12989750 | 23.3% |
反応手順
To a solution of dimethyl methylphosphonate (17.93 g, 144 mmol) in THF (270 mL) at −78° C. was slowly added n-BuLi (2.5M, 64.2 mL, 160.6 mmol). The reaction mixture was stirred for 1 h and (3-chloro-phenyl)-acetic acid methyl ester (26.93 g, 146 mmol) was slowly added. The reaction mixture was allowed to warm to room temperature and was stirred for 24 h. Acetic acid (15 mL) was added and the volatiles were removed in vacuo. The residue was diluted with CH2Cl2 and the organic solution was washed carefully with saturated aqueous NaHCO3 (3 times). The organic layer was dried (MgSO4), filtered and concentrated in vacuo. Purification by medium pressure chromatography (20% EtOAc in hexanes to EtOAc) provided the title compound (9.28 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06747054B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-586da0f17be14ad2b33381744ef6b3e2 |
| 出典メモ | uspto-grants-2004_06 |