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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482907Generated: October 30, 2026

Ammonium formate → (S)-Tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylate

https://huagongshe.com/reaction/1482907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant(S)-tert-butyl 2-(4-(diphenylmethyleneamino)phenyl)morpholine-4-carboxylateHCID 86654632—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(S)-Tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylateHCID 6670598894.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A suspension of (S)-tert-butyl 2-(4-(diphenylmethyleneamino)phenyl)morpholine-4-carboxylate (54.1 g, 122 mmol), ammonium formate (116 g, 1.83 mol) and 5% Pd/C (6.5 g, 3.06 mmol) in methanol (930 ml) was stirred at 60° C. for 2 h. The reaction mixture was filtered and concentrated. The residue was dissolved in ethyl acetate and water. The organic phase was extracted twice with 0.5 M HCl. The combined aqueous phases were basified with 2 M NaOH and extracted twice with DCM. The organic phases were dried over magnesium sulfate, filtered and dried in vacuo, to yield 31.95 g off-white solid. MS (ISP): 279.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416127B2
Source datasetuspto-grants-2016_08
ORD IDord-2463861e02a143708f32be54561b1d69
Source noteuspto-grants-2016_08