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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572703Generated: October 31, 2026

Ammonium formate → HCID 54335918, compound

https://huagongshe.com/reaction/572703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactantα-[[[2-(4-Methoxyphenyl)-1-methylethyl](phenylmethyl)amino]methyl]-3-nitro-4-(phenylmethoxy)benzenemethanolHCID 9914834—
CatalystPalladiumHCID 23938—
ProductHCID 54335918HCID 54335918—

Reaction Conditions

Temperature40 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029421B2
Source datasetuspto-grants-2015_05
ORD IDord-d284eec7e3b34bfdabbeb552d277fce3
Source noteuspto-grants-2015_05