HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404106Generated: November 2, 2026
Diethyl (2-aminoethyl)phosphonate oxalate → HCID 178476908, compound
https://huagongshe.com/reaction/2404106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl (2-aminoethyl)phosphonate oxalate | HCID 2733595 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehyde | HCID 86668412 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178476908 | HCID 178476908 | 36.9% |
Reaction Steps
To a solution of (2-amino-ethyl)-phosphonic acid diethyl ester oxalic acid salt (200 mg, 0.74 mmol) in 1,2-dichloroethane (3 mL) was added 6-(4-tert-butyl-cyclohexyloxy)-naphthalene-2-carbaldehyde (343 mg, 1.1 mmol). The mixture was stirred at room temperature for 1 hour, then sodium triacetoxyborohydride (329 mg, 1.5 mmol) was added. After being stirred at room temperature overnight, the reaction mixture was quenched with water, stirred at room temperature for 30 min, then diluted with ethyl acetate, and washed with aqueous NaHCO3. The organic layer was dried over MgSO4 and purified with a silica gel column eluted with ethyl acetate (100%), then eluted with methanol in dichloromethane from 0 to 15% to give sticky oil (130 mg, yield: 25%). ESI-MS: 476.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802659B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-dc910e067f7f428aa16ce51c097332f0 |
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| Source note | uspto-grants-2014_08 |
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