HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572703Generated: October 31, 2026
Ammonium formate → HCID 54335918, compound
https://huagongshe.com/reaction/572703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | α-[[[2-(4-Methoxyphenyl)-1-methylethyl](phenylmethyl)amino]methyl]-3-nitro-4-(phenylmethoxy)benzenemethanol | HCID 9914834 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 54335918 | HCID 54335918 | — |
Reaction Steps
To a solution of 4-benzyloxy-3-nitro-α-[N-benzyl-N-(1-methyl-2-p-methoxyphenylethyl)aminomethyl]benzyl alcohol (100 gms, 0.19 M) in SPDS (1.0 lit) was added 10% Pd/C. The resulting mass was heated to 40° C. and ammonium formate (36 gms, 0.57 M) was added in lots in 1 hour. The reaction mass was heated slowly to 70° C. for 1 hour, and then cooled to 50° C. The catalyst was removed by filtration and the clear filtrate evaporated. The residue was stirred in water (500 ml) and basified with liq. Ammonia. The reaction mass was extracted in 1.0-lit toluene, washed organic extract with water, dried on sodium sulfate and evaporated to obtain title compound. (78 gms, 83%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029421B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-d284eec7e3b34bfdabbeb552d277fce3 |
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| Source note | uspto-grants-2015_05 |
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