HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 14074730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 14074729 | HCID 14074729 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14074730 | HCID 14074730 | — |
Reaction Steps
To a solution of 4-(triphenylmethylthio)-1-(benzyloxycarbonylhydroxymethyl)azetidin-2-one (1.0 g) and pyridine (240 μl) in tetrahydrofuran (THF) (15 ml) at 0° C. under nitrogen was added slowly thionyl chloride (180 μl ). After 15 minutes the precipitate was collected by filtration and the filtrate evaporated. The residue was rapidly eluted through a short plug of silica gel using a 15 to 30% ethyl acetate/hexane solvent gradient to afford 4-(triphenylmethylthio)-1-(benzyloxycarbonylchloromethyl)azetidin-2-one (900 mg) as a 4:3 mixture of diastereomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04797396 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-cfec8e6f4dfe405a8b63205b824f89a9 |
| Source note | uspto-grants-1989_01 |