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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196847Generated: November 1, 2026

Diethyl chlorophosphate → HCID 86745260, compound

https://huagongshe.com/reaction/1196847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
ReactantHCID 178511996HCID 178511996—
SolventDichloromethaneHCID 6344—
ProductHCID 86745260HCID 86745260—

Reaction Steps

A stirred suspension of 2.94 g (10 mmol) of 1-phenyl-3-(4-phenyl-2-thiazolyl) guanidine (dried at 110° C./0.1 mm) in 150 ml of methylene chloride was allowed to react with 2.03 g (10 mmol) of N,O-bis(trimethylsilyl) acetamide and 1.73 g (10 mmol) of diethyl chlorophosphate for 3 months by the procedure of Example 4. The reaction mixture was evaporated to dryness then was subjected to "dry column" chromatography (method of B. Loev and M. M. Goodman, Chem. and Industry, 2026 (1967) on 500 g of silica gel, and developed with 700 ml of methylene chloride-ethyl acetate, 9/1 (v/v). A band in the Nylon® column at Rf 0.25-0.4, visualized as a dark band under ultraviolet light at 254 nm, was cut out, and extracted with chloroform-methanol, 3/1 (v/v). Evaporation of the extracts left 1.35 g of product as a pale yellow, thick syrup; NMR (CDCl3, 80 MHz) δ 1.37 (t, 6H, CH3), δ 4.11(5 peaks, 4H, OCH2), 6.98 (s, 1H, =CH--S), 7.35(m, 10H, aromatic); IR (neat) 1653 (C=N) and 1032 cm-1 (P=O); TLC (SiO2, CHCl3 --MEOH, 19/1 (v/v)) showed only one spot under UV light.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116827
Source datasetuspto-grants-1992_05
ORD IDord-875397b85f7d4d01b785d171efc0abde
Source noteuspto-grants-1992_05