HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → {5-Hydroxy-4-[(phenylmethyl)oxy]-2-pyridinyl}methyl acetate trifluoroacetate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | {5-({[4-(Methyloxy)phenyl]methyl}oxy)-4-[(phenylmethyl)oxy]-2-pyridinyl}methyl acetate | HCID 67526761 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | {5-Hydroxy-4-[(phenylmethyl)oxy]-2-pyridinyl}methyl acetate trifluoroacetate salt | HCID 67527752 | — |
Reaction Steps
A solution of {5-({[4-(methyloxy)phenyl]methyl}oxy)-4-[(phenyl methyl)oxy]-2-pyridinyl}methyl acetate (containing triphenylphosphine oxide as an impurity) (20 g, 50.8 mmol) in dichloromethane (500 ml) was treated with triethylsilane (10 ml, 62.6 mmol). A solution of trifluoroacetic acid (35 ml, 0.45 mol) in dichloromethane (200 ml) was added over 1 hour. After 2 hours the mixture was evaporated and chromatographed on silica gel eluting with 50-100% ethyl acetate-hexane, then 5-10% methanol-DCM affording a solid, the TFA salt in a 1:1 mixture with triphenylphosphine oxide (8.33 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709483B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-274abda7f633454e8c259a139944d113 |
| Source note | uspto-grants-2010_05 |