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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1599406Generated: November 4, 2026

Formaldehyde → Dimethyl 4-methylaminobenzylphosphonate

https://huagongshe.com/reaction/1599406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantSodiumHCID 5360545—
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 metboxide 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 subsatance. 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 numberUS05741784
Source datasetuspto-grants-1998_04
ORD IDord-7d1d35983e9f4615809093641b13aba1
Source noteuspto-grants-1998_04