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Triethylamine → O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Methyl N-hydroxyethanimidothioate | HCID 92243 | — |
| 反応物 | Phosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl ester | HCID 778771 | — |
| 反応物 | N-chlorothio(methyl)carbamoyl fluoride | HCID 12922862 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate | HCID 86737875 | — |
反応手順
A solution of O,O-diethyl isopropylphosphoramidothioate(14.9 g, 70.8 mmol) and triethylamine (9.8 ml, 70.8 mmol) in tetrahydrofuran (50 ml) is added dropwise over 10 minutes to a solution of N-chlorothio(methyl)carbamoyl fluoride (10.2 g, 70.8 mmol) in tetrahydrofuran (50 ml) cooled in an ice bath. After the addition the mixture is stirred for 1.5 hours at 0°, diluted with ether (200 ml), washed with ice cold water, dried over sodium sulfate and concentrated under reduced pressure. The residue shows identical absorptions in the ir and pmr spectra for νC=O and N--CH3 as obtained for the yellow oil that is intermediate II1 of Example 1. The crude II1 product is suitable for reaction with methyl N-hydroxyethanimidothioate as in Example 1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04336207 |
| 出典データセット | uspto-grants-1982_06 |
| ORD ID | ord-3fc776fce7f74d8bb864eb11f6607529 |
| 出典メモ | uspto-grants-1982_06 |