HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398769Generated: October 29, 2026
3-Chloro-2-chloromethyl-1-propene → (2-Chloromethyl-2-propenyloxymethyl)phosphonic acid diethylester
https://huagongshe.com/reaction/398769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Chloro-2-chloromethyl-1-propene | HCID 15859 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diethyl phosphonomethanol | HCID 76513 | — |
| Reactant | HCID 178449043 | HCID 178449043 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Sodium hydride | HCID 24758 | — |
| Product | (2-Chloromethyl-2-propenyloxymethyl)phosphonic acid diethylester | HCID 54045084 | — |
Reaction Steps
To a mixture of hydroxymethylphosphonic acid diethylester (0.84 g, 5 mmol), 1-chloro-2-chloromethyl-2-propene (0.95 g, 7.6 mmol) and tetrabutylammonium iodine (0.18 g, 0.5 mmol) in anhydrous tetrahydrofuran (10 ml), sodium hydride is added (0.24 g, 6 mmol 60% in oil) at 0° C. The mixture is stirred overnight at 20° C. The reaction mixture is hydrolyzed with a saturated solution of ammonium chloride, extracted with ethyl acetate and the title product is obtained by flash chromatography on silica gel (0.35 g, 27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05817647 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-c4b1974d5efb4fcbb175ef143df02274 |
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| Source note | uspto-grants-1998_10 |
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