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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736383Generated: November 3, 2026

Ammonia → HCID 19707341, compound

https://huagongshe.com/reaction/1736383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhenylacetic AcidHCID 999—
ReactantEthylamineHCID 6341—
ReactantHCID 19707357HCID 19707357—
SolventEthylene GlycolHCID 174—
ProductHCID 19707341HCID 19707341—
ProductHCID 54248187HCID 54248187—

Reaction Steps

By following the procedures described in Example 40, Steps A, B, C, D, E and F using phenylacetic acid as the starting material and using ethylamine rather than ammonia, and digylme rather ethylene glycol in Step F, the compound 4-ethyl-10b-methyl-1,2,3,4,6,10b-hexahydrobenzo[f]quinolin-3-one was prepared. This hexahydrobenzo[f]quinolin-3-one was hydrogenated by following the procedures described Example 22 except that the reaction was carried out at 70° C. over 7 hours to afford a crude reaction mixture. The reaction mixture was filtered and the solvents evaporated under vacuum to afford a glassy solid residue. The crude product was purified by chromatography on SiO2 (gradient elution from 100% hexanes to 100% CHCl3) to afford 92 mg of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541190
Source datasetuspto-grants-1996_07
ORD IDord-f62f1846425c47e2a4dae64db6b8ab3e
Source noteuspto-grants-1996_07