HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916229Generated: October 25, 2026
Ethanol → (R)-3-(3-Fluorophenoxy)-3-phenylpropylamine
https://huagongshe.com/reaction/916229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | (R)-3-(3-Fluorophenoxy)-3-phenylpropylchloride | HCID 39364375 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (R)-3-(3-Fluorophenoxy)-3-phenylpropylamine | HCID 11593957 | — |
Reaction Steps
A solution of (R)-3-(3-fluorophenoxy)-3-phenylpropyl chloride (0.971 g, 3.96 mmol), conc. NH4OH (30 mL), and EtOH (20 mL) were shaken at 90° C. on a Parr apparatus (50-90 psig) for 18 h. The mixture was then evaporated under vacuum and the residue was dissolved in Et2O (100 mL) and washed with H2O (2×25 mL). The organic layer was dried (anh. Na2SO4), filtered, and evaporated under vacuum to provide a yellow oil. This material was then dissolved in EtOAc (50 mL) and filtered. A solution of 30 maleic acid (0.272 g, 2.6 mmol, 0.93 equiv) dissolved in hot EtOAc (5 mL) was added to precipitate the maleate salt (519 mg, 53.5%) as a white solid: TLC Rf 0.25 (1% MeOH—CHCl3); GC, tr 7.37 min; MS, m/z 245 (M+). The synthesis of Compound 187 was accomplished as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268166B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-455e585efe2b47ad951d4e795d65e509 |
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| Source note | uspto-grants-2007_09 |
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