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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1156502Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethyl N-hydroxyethanimidothioateHCID 92243—
EduktPhosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl esterHCID 778771—
EduktN-chlorothio(methyl)carbamoyl fluorideHCID 12922862—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktO,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioateHCID 86737875—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04336207
Quelldatensatzuspto-grants-1982_06
ORD IDord-3fc776fce7f74d8bb864eb11f6607529
Quellennotizuspto-grants-1982_06