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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713887Generated: November 4, 2026

Diethyl (2-aminoethyl)phosphonate oxalate → HCID 178476908, compound

https://huagongshe.com/reaction/713887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (2-aminoethyl)phosphonate oxalateHCID 2733595—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant6-(trans-4-Tert-butylcyclohexyloxy)-2-naphthaldehydeHCID 86668412—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178476908HCID 17847690836.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186367B2
Source datasetuspto-grants-2015_11
ORD IDord-f327ffd01c404b969bff2e61a2120865
Source noteuspto-grants-2015_11