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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2252048Generated: November 2, 2026

HCID 69212492, compound → HCID 85937142, compound

https://huagongshe.com/reaction/2252048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69212492HCID 69212492—
CatalystHCID 178418406HCID 178418406—
SolventAcetonitrileHCID 6342—
ProductHCID 85937142HCID 8593714252%

Reaction Steps

Dissolve 4-(N-tert-butoxycarbonyl-N-ethyl-amino)-benzyl alcohol (1.24 g, 5.52 mmol) in 50 mL acetonitrile. Add to this solution manganese dioxide and stir the mixture for two days at room temperature. Filter the residue through Celite® and concentrate the solvent to give 632 mg of 4-(N-tert-butoxycarbonyl-N-ethyl-amino) benzaldehyde. Yield 52%. 1H-NMR (CDCl3, 300 MHz): 9.95 (s, 1H); 7.83 (d, J=8.7 Hz, 2H); 7.39 (d, J=8.7 Hz, 2H); 3.74 (q, J=7.0 Hz, 2H); 1.45 (s, 9H); 1.18 (t, J=7.0 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07320995B2
Source datasetuspto-grants-2008_01
ORD IDord-ab1ad4fb6bab470182ec80f4340d0257
Source noteuspto-grants-2008_01