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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | (S)-tert-butyl 2-(4-(diphenylmethyleneamino)phenyl)morpholine-4-carboxylate | HCID 86654632 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-Tert-butyl 2-(4-aminophenyl)morpholine-4-carboxylate | HCID 66705988 | 94.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416127B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-2463861e02a143708f32be54561b1d69 |
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| Source note | uspto-grants-2016_08 |
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