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Dimethylformamide → (Chloro(phenylmethoxy)phosphoryl)oxymethylbenzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Oxalyl chloride | HCID 65578 | — |
| 反応物 | Dibenzylphosphate | HCID 4193600 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (Chloro(phenylmethoxy)phosphoryl)oxymethylbenzene | HCID 4641201 | — |
反応手順
A solution of dibenzyl phosphate (3.76 g, 13.5 mmol) in CH2Cl2 (10 mL) was treated with oxalyl chloride (1.17, 13.5 mmol) and DMF (0.5 mL). The mixture was stirred at room temperature for 1 h, the solvent was removed by rotary evaporation and the residue was dried in vacuo for 2 h to afford dibenzyl chlorophosphate as a yellowish solid. The residue was suspended in CH2Cl2 (5 mL), cooled to 0° C., treated with a solution of benzylic alcohol M (1.7 g, 6.7 mmol) in CH2Cl2 (5 mL) then DBU (2.02 mL, 13.5 mmol, added dropwise). The mixture was stirred at room temperature for 1 h30, and the solvent was removed by rotary evaporation. The residue was purified by column chromatography over silica gel using a gradient of 0-10% EtOAc/hexane as eluent.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07425553B2 |
| 出典データセット | uspto-grants-2008_09 |
| ORD ID | ord-37b1cc5b621449d489a8afc96a527baa |
| 出典メモ | uspto-grants-2008_09 |