Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | HCID 86657604 | HCID 86657604 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 86657603 | HCID 86657603 | 85% |
Reaction Steps
At room temperature, 2.3 g (0.06 mol) of lithium aluminohydride in 100 ml of 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 22.0 g (0.1 mol) of butyl ethyl(2-methyl-2-formylethyl)phosphinate in 100 ml of diethyl ether added dropwise at such a rate that there is a moderate boil of the diethyl ether. On completion of the dropwise addition the reaction solution is refluxed for 1 hour and subsequently admixed with 1.8 g (0.1 mol) of water. The insoluble salts are filtered off. The solvent of the filtrate is removed in vacuo and the product is purified by chromatography to obtain 18.9 g (85% of theory) of butyl ethyl(2-methyl-3-hydroxypropyl)phosphinate as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604108B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-62785e42a81a4d87801f27caf1db4666 |
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| Source note | uspto-grants-2013_12 |
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