HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484000Generated: October 31, 2026
Acetic Acid → 3-(p-Chlorobenzylamino)propyl(n-butyl)phosphinic acid ethyl ester
https://huagongshe.com/reaction/484000
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 3-Aminopropyl(n-butyl)phosphinic acid ethyl ester | HCID 9990598 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(p-Chlorobenzylamino)propyl(n-butyl)phosphinic acid ethyl ester | HCID 53755720 | — |
Reaction Steps
4.14 g of 3-aminopropyl(n-butyl)phosphinic acid ethyl ester are mixed with 2.51 g of p-chlorobenzaldehyde, and first 1.2 g of glacial acetic acid and then a solution of 0.42 g of sodium cyanoborohydride in 5 ml of methanol are added, whereupon an exothermic reaction takes place. The mixture is then stirred at room temperature for 2.5 hours and adjusted to pH 8, and the volatile constituents are removed under reduced pressure. The residue is dissolved in dichloromethane, washed with water, dried over sodium sulfate and concentrated by evaporation. The residue is purified by chromatography on silica gel, yielding 3-(p-chlorobenzylamino)propy(n-butyl)phosphinic acid ethyl ester; 1H-NMR spectrum (in CDCl3): δ=7.30-7.32 (4H,m); 4.02 (2H,q); 3.74 (2H,s); 2.67 (2H,t); 2.5-2.22 (1H,S); 1.79-1.64 (6H,m); 1.53 (2H,m); 1.42 (2H,m); 1.31 (3H,t); 0.81 (3H,t); 31P-NMR spectrum (in CDCl3 ): δ=58.16.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05229379 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-25fd38d5bc304be982bc64fa74039ef9 |
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| Source note | uspto-grants-1993_07 |
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