Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methyl N-hydroxyethanimidothioate | HCID 92243 | — |
| 반응물 | Phosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl ester | HCID 778771 | — |
| 반응물 | N-chlorothio(methyl)carbamoyl fluoride | HCID 12922862 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate | HCID 86737875 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04336207 |
| 출처 데이터셋 | uspto-grants-1982_06 |
| ORD ID | ord-3fc776fce7f74d8bb864eb11f6607529 |
| 출처 메모 | uspto-grants-1982_06 |