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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014389Generated: November 1, 2026

Formaldehyde → 1,1-Dimethylethyl [5-(methylamino)-2-(methyloxy)phenyl]carbamate

https://huagongshe.com/reaction/1014389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactanttert-butyl N-(5-amino-2-methoxyphenyl)carbamateHCID 22344747—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
Product1,1-Dimethylethyl [5-(methylamino)-2-(methyloxy)phenyl]carbamateHCID 59441835104.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 1,1-dimethylethyl [5-amino-2-(methyloxy)phenyl]carbamate (1.94 g, 8.14 mmol), paraformaldehyde (1.222 g, 40.7 mmol), and sodium methoxide (2.199 g, 40.7 mmol) in methanol (50 ml) was maintained at 50° C. for 16 hours, cooled, sodium borohydride (0.924 g, 24.42 mmol) was added portionwise, and the solution was re-heated to 50° C. and maintained for an additional 24 hours. The solution was cooled, diluted with ethyl acetate, saturated sodium bicarbonate, and the organic layer was dried over sodium sulfated, filtered, taken to a residue under reduced pressure, and purified by column chromatography to afford 1,1-dimethylethyl [5-(methylamino)-2-(methyloxy)phenyl]carbamate (2.15 g, 8.52 mmol, quant. Yield) as a pale yellow oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.58 (s, 1 H), 7.10 (d, J=1.6 Hz, 1 H), 6.76 (d, J=8.8 Hz, 1 H), 6.14 (dd, J=8.7, 2.7 Hz, 1H), 5.07-5.31 (m, 1 H), 3.61-3.74 (m, 3 H), 2.60 (d, J=4.4 Hz, 3 H), 1.44 (s, 9 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981903B2
Source datasetuspto-grants-2011_07
ORD IDord-86ff43889252450e9139978a77ad0a01
Source noteuspto-grants-2011_07