戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1156502作成日:2026年10月24日

Triethylamine → O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate

https://huagongshe.com/ja/reaction/1156502

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methyl N-hydroxyethanimidothioateHCID 92243—
反応物Phosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl esterHCID 778771—
反応物N-chlorothio(methyl)carbamoyl fluorideHCID 12922862—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioateHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04336207
出典データセットuspto-grants-1982_06
ORD IDord-3fc776fce7f74d8bb864eb11f6607529
出典メモuspto-grants-1982_06