HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 10685511, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Chloro-3-pyridinol | HCID 81136 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | tert-butyl (2S)-2-(hydroxymethyl)azetidine-1-carboxylate | HCID 10511797 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10685511 | HCID 10685511 | 37.2% |
Reaction Steps
To a solution of triphenylphosphine (1.73 g, 6.6 mmol) in THF (26 mL) was added diethyl azodicarboxylate (1.04 mL, 6.6 mmol) at 0° C., and the reaction mixture was stirred for 15 minutes. 1-BOC-2-(S)-azetidinemethanol (1.03 g, 5.5 mmol) and 2-chloro-3-pyridinol (785 mg, 6.0 mmol, Aldrich Chemical Co.) were then added. The reaction mixture was allowed to warm slowly to room temperature and stir overnight. Solvent was removed, and the residue was dissolved in ethyl acetate. The solution was washed with saturated aqueous K2CO3 and brine, dried over MgSO4 and concentrated. The residue was chromatographed on a silica gel column, eluting with ethyl acetate:hexane (1:4 to 1:1) to afford the title compound (611 mg). MS (DCI/NH3) m/z 299 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133253 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-eee07a24dfb041d4bd12688d0d85b886 |
| Source note | uspto-grants-2000_10 |