HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229110Generated: October 25, 2026
Methyl Acetate → (r)-2-(3-{3-[[3-Fluoro-4-methoxybenzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}phenyl)acetic acid hydrochloride salt
https://huagongshe.com/reaction/229110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Acetate | HCID 6584 | — |
| Reactant | 3-Fluoro-p-anisaldehyde | HCID 67696 | — |
| Reactant | 2-Chloro-3-(trifluoromethyl)benzaldehyde | HCID 2736672 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | (R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}phenyl)acetic acid | HCID 68864815 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (r)-2-(3-{3-[[3-Fluoro-4-methoxybenzyl](2,2-diphenylethyl)amino]-1-methyl-propoxy}phenyl)acetic acid hydrochloride salt | HCID 68865443 | — |
Reaction Steps
Following the procedure of Example 7(d) except (R)-2-(3-{3-[(2,2-diphenylethyl)amino]-1-methyl-propoxy}-phenyl)acetic acid and 3-fluoro-4-methoxybenzaldehyde were used instead of (R)-2-(3-{3-(2,2-diphenylethyl)amino]-3-methyl-propoxy}-phenyl)acetic acid methyl ester and 2-chloro-3-trifluoromethylbenzaldehyde in step (d) the corresponding carboxylic acid was obtained. The crude product was purified by preparative HPLC (TMC CombiPrep PDS, 75×30 mm, 25 mL/min, acetonitrile: H2O, UV detection at 254 nm) to afford the free base. The resulting amine/carboxylic acid was dissolved in Et2O (diethylether) and acidified with 1.0 M HCl/Et2O. The reaction mixture was concentrated in vacuo and dried under reduced pressure to give the title compound as a white solid, 100 mg (99%). MS (ESI) 542.4 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560586B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-e48897df6d804999a2850913760af972 |
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| Source note | uspto-grants-2009_07 |
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