HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114331Generated: October 27, 2026
Acetic Acid → [1-(4-Biphenylyl)-2-(4-morpholinyl)ethyl]methylamine
https://huagongshe.com/reaction/2114331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(4-Biphenylyl)-2-(4-morpholinyl)ethanone | HCID 57418661 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [1-(4-Biphenylyl)-2-(4-morpholinyl)ethyl]methylamine | HCID 57425536 | 53% |
Reaction Steps
2.0 M methylamine solution in THF (18 mL, 36.0 mmol) was added to a solution of 1-(4-biphenylyl)-2-(4-morpholinyl)ethanone (2.52 g, 8.93 mmol ) in anhydrous THF (20 mL), The reaction mixture was stirred at room temperature for 1 h and then sodium cyanoborohydride (1.68 g, 26.79 mmol) and acetic acid (1 mL) were added. The resulting mixture was stirred at room temperature for 72 h until the starting material was consumed completely. At this point, saturated K2CO3 solution (40 mL) was added to and after stirring for 15 min, the solution was extracted with ethyl acetate (2×50 mL). The combined organic layer was dried over Na2SO4 and concentrated. The resulting residue was isolated by column chromatography on silica gel (MeOH/EtOAc, 1:10) to yield [1-(4-biphenylyl)-2-(4-morpholinyl)ethyl]methylamine as an off-white solid(1.40 g, 53%), MS (ES) m/e 296[M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432258B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-17343c333cef4a60a2068314515f0eb4 |
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| Source note | uspto-grants-2008_10 |
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