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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1277899Generated: October 25, 2026

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

https://huagongshe.com/reaction/1277899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl N-hydroxyethanimidothioateHCID 92243—
ReactantPhosphoramidothioic acid, (1-methylethyl)-, O,O-diethyl esterHCID 778771—
ReactantN-chlorothio(methyl)carbamoyl fluorideHCID 12922862—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductO,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioateHCID 86737875—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04279840
Source datasetuspto-grants-1981_07
ORD IDord-3db82a83e41c4907aabdc252be4c7754
Source noteuspto-grants-1981_07