HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 89348460, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Acetyl-L-phenylalanine | HCID 74839 | — |
| Reactant | N-Methylmercaptoacetamide | HCID 100435 | — |
| Reactant | (DIPHENYLPHOSPHINO)METHANETHIOL | HCID 11230015 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 89348460 | HCID 89348460 | 92% |
Reaction Steps
Method A (transthioesterification). Phosphinothiol 20 (500 mg, 2.2 mmol) was dissolved in dry TBF (5 mL). The solution was deoxygenated by bubbling Ar(g) for 0.5 h. To this solution was added NaH (51.6 mg, 2.2 mmol). The mixture formed a slurry to which was added DMF (2 mL0 to dissolve any precipitate. The N-methylmercaptoacetamide (NMA) thioester of N-acetylphenylalanine (63 mg, 0.22 mmol) was added, and the reaction mixture was stirred for 8 h. Unreacted Phosphinothiol 20 was removed by adding Merrifield resin (1.5 g, 1.26 mmol/g), stirring for 6 h, and removing the resin by filtration. The residue was purified by flash chromatography (silica gel, 50% ethyl acetate in hexanes). AcPheSCH2PPh2 was isolated as a white solid in 92% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06972320B2 |
| Source dataset | uspto-grants-2005_12 |
| ORD ID | ord-d2edf7045dc54591938d7e7c3d47f087 |
| Source note | uspto-grants-2005_12 |