関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | p-Toluenesulfonyl azide | HCID 13661 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | Dimethyl (2-oxopropyl)phosphonate | HCID 77872 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (1E)-1-diazo-1-dimethoxyphosphorylpropan-2-one | HCID 136023029 | 92.3% |
反応手順
To sodium hydride (188 mg of a 60% solution in mineral oil, 113 mg clean, 4.70 mmol) in 14 mL of benzene and 2.5 mL of tetrahydrofuran, add (2-oxo-propyl)-phosphonic acid dimethyl ester (743 mg, 618 μL, 4.48 mmol) as a solution in 5 mL of benzene at 0° C. dropwise. The mix remains white and produces some gas. After 1 h at 0° C., add tosyl azide (940 mg, 4.70 mmol) as a solution in 2.5 mL of benzene and warm the mixture to RT. After 2.3 hours, pour the mix through a plug of Celite® rinsing with tetrahydrofuran, benzene, and ether. Concentrate the filtrate and purify the residue by chromatography (Hexanes/EtOAc gradient) to provide 794 mg of (1-Diazo-2-oxo-propyl)-phosphonic acid dimethyl ester as a yellow solid. This material may be used directly. Exact Mass 192.03: mass spectrum (aspci): m/z=165.0 (M+1 (—N2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07179804B2 |
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| 出典データセット | uspto-grants-2007_02 |
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| ORD ID | ord-448579858ec84eaab26152e38ed1daae |
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| 出典メモ | uspto-grants-2007_02 |
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