HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742397Generated: October 30, 2026
Hydrochloric Acid → HCID 19425294, compound
https://huagongshe.com/reaction/742397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Octylamine | HCID 8143 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide | HCID 15279390 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 19425294 | HCID 19425294 | 30.2% |
Reaction Steps
N-(2-Fluoro-4-chloro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide (1.00 g, 2.75 mmol), octylamine (0.460 g, 3.56 mmol), triethylamine (0.310 g, 3.06 mmol) and benzene (25 ml) as a solvent were placed into a round bottom flask (50 cc) and stirred overnight at room temperature. After completion of the reaction, the reaction mixture was poured into 1N hydrochloric acid (50 ml), and the mixture was extracted with ethyl acetate (50 ml×3 portions). The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resulting crude product was recrystallized from ether to obtain N-(2-fluoro-4-chloro-5-cyclopentyloxyphenyl)-N'-octyl-3,4,5,6-tetrahydrophthalamide as white crystals (0.410 g, 30.2% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554581 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-0ed99584cb87444e9a179586f05f2b12 |
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| Source note | uspto-grants-1996_09 |
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