HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196847Generated: November 1, 2026
Diethyl chlorophosphate → HCID 86745260, compound
https://huagongshe.com/reaction/1196847
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | HCID 178511996 | HCID 178511996 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86745260 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116827 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-875397b85f7d4d01b785d171efc0abde |
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| Source note | uspto-grants-1992_05 |
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