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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079315Generated: November 2, 2026

Formaldehyde → Dimethyl 4-methylaminobenzylphosphonate

https://huagongshe.com/reaction/1079315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
ReactantDimethyl [(4-aminophenyl)methyl]phosphonateHCID 12843961—
SolventMethanolHCID 887—
ProductDimethyl 4-methylaminobenzylphosphonateHCID 1892807713%

Reaction Steps

Dimethyl 4-aminobenzylphosphonate (21.5 g) and then paraformaldehyde (80%, 5.3 g) were added at room temperature to a solution of sodium methoxide in methanol (prepared from 27 g of sodium and 250 ml of methanol). After this mixture was stirred at room temperature for 15 hours, sodium borohydride (3.8 g) was added, and the mixture was heated for 1.5 hours while refluxing. The reaction mixture was concentrated under reduced pressure and then the residue was treated with 1NKOH (500 ml) and extracted with chloroform. The chloroform layer was washed with water and dried (MgSO4), after which the solvent was distilled off. The residue was subjected to silica gel column chromatography and eluted with ethyl acetate-chloroform-methanol (25:25:1, v/v) to yield dimethyl 4-methylaminobenzylphosphonate (2.9 g, 13%) as an oily substance. NMR(δ ppm in CDCl3): 2.55(1H,broad s), 2.82(3H,s), 3.07(2H,d,J=21 Hz), 3.63(3H,s), 3.69(3H,s), 6.57(2H,dd,J=9&1 Hz), 7.11(2H,dd,J =9&3 Hz)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580863
Source datasetuspto-grants-1996_12
ORD IDord-fdc6df87e4cc4beda357a7499944f946
Source noteuspto-grants-1996_12