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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026782Generated: October 26, 2026

(S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-one → (S)-3-(dimethylamino)-2-methyl-1-(3-aminophenyl)-propan-1-one

https://huagongshe.com/reaction/1026782

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-oneHCID 53235125—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
Solvent2-MethyltetrahydrofuranHCID 7301—
Product(S)-3-(dimethylamino)-2-methyl-1-(3-aminophenyl)-propan-1-oneHCID 5323504698%

Reaction Conditions

Temperature2 °C

Reaction Steps

(S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-one (100 g, 0.423 mol), methyl-tetrahydrofuran (400 ml) and Pd/C 5%, anhydrous (4.0 g) are added into a 1 liter autoclave, at room temperature. The suspension is cooled to 0-4° C., then it is hydrogenated at 2 bars of hydrogen gas without exceeding 8° C. The conversion is monitored using HPLC and it is deemed complete when the HPLC area % of the initial product and the reaction intermediates is <0.3. Then catalyst is filtered and the solution can be used as it is in the subsequent step or concentrated under vacuum at 45-50° C. to oily residue. About 86 g of yellow to dark red oil are obtained (about 98% yield, ee≧97%, purity ≧92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729308B2
Source datasetuspto-grants-2014_05
ORD IDord-d7d84980df514c30a53700661604aadf
Source noteuspto-grants-2014_05