HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(4-Benzyl-morpholin-2-yl)-2-chloro-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 4-Benzyl-6-(3-chloro-4-hydroxy-phenyl)-morpholin-3-one | HCID 66653719 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Benzyl-morpholin-2-yl)-2-chloro-phenol | HCID 66654072 | 76.8% |
Reaction Steps
To a solution of 4-benzyl-6-(3-chloro-4-hydroxy-phenyl)-morpholin-3-one (13.05 g; 39.0 mmol) in THF (600 mL) was added portionwise LiAlH4 (4.44 g; 117.04 mmol) at 0° C. The resulting mixtures was allowed to warm to RT and stirred overnight. Subsequently, the mixture was cooled to 0° C., and water (4.5 mL), a 2M aqueous NaOH-solution (9.0 mL) and water (9.0 mL) were added consecutively. Thereafter the mixture was stirred for 1 h. The formed precipitate was removed by filtration over kieselguhr, and washed with EtOAc. The organic solution was concentrated in vacuo, and the residue purified by column chromatography (SiO2, CH2Cl2/MeOH 98:2) to afford 4-(4-benzyl-morpholin-2-yl)-2-chloro-phenol (9.10 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09227960B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-4ce2480c91514aff9b475c1d8c26c73c |
| Source note | uspto-grants-2016_01 |