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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014385Generated: October 30, 2026

Formaldehyde → 1208091-01-3

https://huagongshe.com/reaction/1014385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-Methyl-4-methoxyanilineHCID 7610—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product1208091-01-3HCID 1456781491.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of [2-methyl-4-(methyloxy)phenyl]amine (5 ml, 39.2 mmol), paraformaldehyde (5.88 g, 196 mmol), and sodium methoxide (10.58 g, 196 mmol) in methanol (100 ml) was maintained at 50° C. for 5 hours, cooled, and sodium borohydride (7.41 g, 196 mmol) was added portionwise. The resulting suspension was re-heated to 50° C. and maintained for 16 hours. The reaction was cooled, poured into ethyl acetate/saturated sodium bicarbonate, and the organic layer was dried over sodium sulfate, filtered, taken to a residue under reduced pressure, and purified by column chromatography to afford N,2-dimethyl-4-(methyloxy)aniline (5.40 g, 35.7 mmol, 91% yield) as a pale orange oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 6.55-6.68 (m, 2 H), 6.34-6.40 (m, 1 H), 4.47-4.66 (m, 1 H), 3.62 (s, 3 H), 2.66 (d, J=5.0 Hz, 3 H), 2.04 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-8092586925c54cfb88c9bd4dbcf0fc53
Source noteuspto-grants-2011_07