HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576016Generated: October 26, 2026
Water → Butyl ethyl(2-methyl-3-aminopropyl)phosphinate
https://huagongshe.com/reaction/576016
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Butyl ethyl(2-cyano-2-methylethyl)phosphinate | HCID 86657307 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Butyl ethyl(2-methyl-3-aminopropyl)phosphinate | HCID 46212766 | 85% |
Reaction Steps
At room temperature, 2.3 g (0.06 mol) of lithium aluminum hydride in 100 ml absolute diethyl ether in a three-neck flask equipped with stirrer, dropping funnel and high-performance condenser are, while continuously stirring, admixed with a solution of 21.7 g (0.1 mol) of butyl ethyl(2-cyano-2-methylethyl)phosphinate (produced similarly to Example 10) in 100 ml of diethyl ether added dropwise at such a rate that there is a moderate boil of the diethyl ether. This is followed by refluxing for 1 hour and admixing of the reaction solution with 1.8 g (0.1 mol) of water, and the insoluble salts are filtered off, the solvent is removed in vacuo and the product is purified by chromatography to obtain 18.8 g (85% of theory) of butyl ethyl(2-methyl-3-aminopropyl)phosphinate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09035088B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-7e10142155f94469bce8953c91e76543 |
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| Source note | uspto-grants-2015_05 |
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