HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583141Generated: October 25, 2026
Methane → N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-diethylamino-benzamide
https://huagongshe.com/reaction/583141
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methane | HCID 297 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-(3,3-dichloro-1-ethyl-1-methyl-2-oxopropyl)-4-diethylaminobenzamide | HCID 17760243 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-diethylamino-benzamide | HCID 17760188 | 76.6% |
Reaction Steps
The N-(3,3-dichloro-1-ethyl-1-methyl-2-oxopropyl)-4-diethylaminobenzamide (390 mg) prepared in the previous step, 50 mL of ethanol and 75 mg of 5% palladium over charcoal were placed in a hydrogenation bottle and hydrogenated in a Parr apparatus (50 psia, room temperature) for 3 hours. The reaction mixture was filtered through celite and the solvent eliminated under reduced pressure, to yield a crude product. The crude product was dissolved in ethyl acetate and then shaken with saturated aqueous sodium bicarbonate. The phases were separated and the organic layer was dried over anhydrous magnesium sulfate. The solvent was then eliminated using a rotary evaporator, yielding 270 mg N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-diethylamino-benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05929098 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-c169eefbc364458d930eb4ee2fedb99a |
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| Source note | uspto-grants-1999_07 |
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