HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine, 4-(chloroacetyl)- → HCID 178521450, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine, 4-(chloroacetyl)- | HCID 74040 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Reactant | HCID 178521541 | HCID 178521541 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178521450 | HCID 178521450 | 100% |
Reaction Steps
A suspension of trans-4-[6-(cyclopropylmethoxy)-1-benzofuran-2-yl]cyclohexanol (611 mg), 4-(chloroacetyl)morpholine (1.05 g) and tert-butoxy potassium (718 mg) in THF (10 mL) was stirred at room temperature overnight and extracted with ethyl acetate and water. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (882 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08703758B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-b7569095f45042ba8d9be37b80a292c7 |
| Source note | uspto-grants-2014_04 |