HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114417Generated: October 31, 2026
Methylamine → [(1R)-1-(4-bromophenyl)-2-(4-morpholinyl)ethyl]methylamine
https://huagongshe.com/reaction/2114417
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-[(2R)-2-(4-bromophenyl)-2-chloroethyl]morpholine | HCID 59809618 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [(1R)-1-(4-bromophenyl)-2-(4-morpholinyl)ethyl]methylamine | HCID 57425542 | 93% |
Reaction Steps
Crude 4-[(2R)-2-(4-Bromophenyl)-2-chloroethyl]morpholine (34.5 g) was dissolved in 200 mL of EtOH at room temperature with magnetic stirring. The resulting solution was cooled to 0° C. and treated with MeNH2 (71 mL, 33 wt % in EtOH) under N2. The reaction flask was capped with a rubber septum and the reaction mixture maintained at room temperature for 48 h. The mixture was then concentrated and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The organic layer was washed with brine, dried over MgSO4, and filtered. The filtrate was concentrated to yield the title compound as a yellow solid (32 g, 93%). MS (ES) m/e 300 [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-df4888b4b1174495af4c2839637c72f6 |
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| Source note | uspto-grants-2008_10 |
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