HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440679Generated: October 26, 2026
Acetic Acid → 3-(3,5-Dichloro-benzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester
https://huagongshe.com/reaction/1440679
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,5-Dichlorobenzaldehyde | HCID 35746 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Phosphinic acid, (3-aminopropyl)(diethoxymethyl)-, ethyl ester | HCID 10422382 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(3,5-Dichloro-benzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester | HCID 21805327 | — |
Reaction Steps
1.41 g of 3,5-dichlorobenzaldehyde are added to a solution of 2.53 g of 3-aminopropyl(diethoxymethyl)phosphinic acid ethyl ester in 10 ml of anhydrous methanol and the resulting clear solution is stirred at room temperature for 30 minutes. There are then added first 0.6 g of glacial acetic acid and then, dropwise, 0.21 g of sodium cyanoborohydride dissolved in 5 ml of methanol. An exothermic reaction begins. The reaction mixture is stirred for 3 hours at 20°, adjusted to pH 8, and the solvent is removed. The residue is dissolved in dichloromethane and washed with water. The organic phase is separated off, dried over sodium sulfate and concentrated to dryness by evaporation. The oil that remains behind is purified by chromatography on silica gel, yielding 3-(3,5-dichloro-benzylamino)propyl(diethoxymethyl)phosphinic acid ethyl ester in the form of a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05500418 |
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| Source dataset | uspto-grants-1996_03 |
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| ORD ID | ord-f5a11c96ee764f5d8068c202acbb25df |
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| Source note | uspto-grants-1996_03 |
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