HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079315Generated: November 2, 2026
Formaldehyde → Dimethyl 4-methylaminobenzylphosphonate
https://huagongshe.com/reaction/1079315
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Dimethyl [(4-aminophenyl)methyl]phosphonate | HCID 12843961 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Dimethyl 4-methylaminobenzylphosphonate | HCID 18928077 | 13% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05580863 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-fdc6df87e4cc4beda357a7499944f946 |
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| Source note | uspto-grants-1996_12 |
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