HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-[3-(4-Bromophenyl)propyl]morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 3-(4-Bromophenyl)-1-morpholinopropan-1-one | HCID 22179856 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-(4-Bromophenyl)propyl]morpholine | HCID 22179832 | 78% |
Reaction Steps
A solution of Example 4B (760 mg, 2.550 mmol) in THF (10 mL) at room temperature was treated with 5M BH3/dimethylsulfide in diethyl ether (2.55 mL, 12.752 mmol), stirred for 24 hours, treated with 3N aqueous HCl (10 mL), heated to reflux for 1 hour, and partitioned between ethyl acetate and 1N NaOH. The aqueous layer was extracted with ethyl acetate (3×50 mL) and the combined extracts were dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 5% 2N NH3 in methanol/dichloromethane to provide the desired product (565 mg, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07358251B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-11c71f7a035f4c30beca4ae9f68d0e0f |
| Source note | uspto-grants-2008_04 |