HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-hydroxy-2-(4-iodophenyl)ethyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl dichloroacetate | HCID 10808 | — |
| Reactant | (2S,1R)-2-Amino-3-fluoro-1-(4-iodo-phenyl)-propan-1-ol | HCID 45257860 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,2-dichloro-N-[(1S,2R)-1-(fluoromethyl)-2-hydroxy-2-(4-iodophenyl)ethyl]acetamide | HCID 68350473 | 73.1% |
Reaction Steps
To a solution of commercially available (1R,2S)-2-amino-3-fluoro-1-(4-iodophenyl)propan-1-ol (5.0 g, 20.0 mmol) in methanol (100 mL) is added triethylamine (9.56 mL, 67.8 mmol) and ethyldichloroacetate (6.22 mL, 50.8 mmol) and the mixture heated to reflux for 16 hours. After allowing to cool to room temperature, the solvent is removed under reduced pressure the resultant oil purified by column chromatography eluting from neat heptanes to 80% ethylacetate/heptanes to give the title compound (5.94 g). m/z (Cl) M+H 405.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09145355B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-45c830550d0e4c1fba94fc154b454d2f |
| Source note | uspto-grants-2015_09 |