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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (S)-3-(dimethylamino)-2-methyl-1-(3-nitro-phenyl)-propan-1-one | HCID 53235125 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Product | (S)-3-(dimethylamino)-2-methyl-1-(3-aminophenyl)-propan-1-one | HCID 53235046 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729308B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-d7d84980df514c30a53700661604aadf |
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| Source note | uspto-grants-2014_05 |
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