HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 4-Benzyl-2-(2-chloro-4-fluoro-phenyl)morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | 2-Chloro-4-fluorophenacyl bromide | HCID 12593335 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Benzyl-2-(2-chloro-4-fluoro-phenyl)morpholine | HCID 89726115 | 99.7% |
Reaction Steps
Combine formic acid (98-100%; 0.30 mL, 8 mmol) and 2-benzylaminoethanol (1.21 g, 8 mmol) and cool the resulting mixture with an ice bath. Add 2-bromo-1-(2-chloro-4-fluoro-phenyl)ethanone (1.0 g, 4 mmol); heat the mixture to reflux; and stir at that temperature for 20 h. Dilute the mixture with DCM and wash with saturated aqueous Na2CO3 solution. Dry organic phases over MgSO4; filter; collect the filtrate; and concentrate under reduced pressure. Purify via flash column chromatography eluting with a gradient of 0-20% methyl tertiary-butyl ether in hexanes. Combine the product fractions and remove the solvents under reduced pressure to give the title compound as a yellow oil (1.22 g, 43%). MS (m/z): 306 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993568B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-dcceaae92c9a49aa93eed45e0fab0345 |
| Source note | uspto-grants-2015_03 |