HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542299Generated: October 27, 2026
Hydrochloric Acid → Ethyl (3-aminobutyl)(diethoxymethyl)phosphinate
https://huagongshe.com/reaction/542299
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Ethyl 3-oxobutyl(diethoxymethyl)phosphinate | HCID 14362820 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl (3-aminobutyl)(diethoxymethyl)phosphinate | HCID 14362822 | — |
Reaction Steps
To a solution of 8.0 g of ethyl 3-oxobutyl(diethoxymethyl)phosphinate in 100 ml of methanol is added 22.8 g of ammonium acetate and 1.3 g of sodium cyanoborohydride. The mixture is stirred under an atmosphere of nitrogen at room temperature for a period of 2.5 h, and then left to stand overnight. The mixture is then acidified to pH 2 with the requisite amount of dilute hydrochloric acid and the methanol is evaporated under reduced pressure. The crude product is dissolved in 25 ml of water, washed twice with 20 ml of diethyl ether and the aqueous phase is then made alkaline to pH 12 with potassium hydroxide. The solution is then saturated with sodium chloride and extracted with 3×25 ml of dichloromethane. The organic phase is dried over magnesium sulphate, filtered and evaporated under reduced pressure and the crude product distilled to give ethyl 3-aminobutyl(diethoxymethyl)phosphinate, b.p. 150° C./0.01 mbar, 31P=+46.1 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04656298 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-bbb5cf4121374153bd61759b09581164 |
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| Source note | uspto-grants-1987_04 |
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