HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → HCID 56987241, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 53999217 | HCID 53999217 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56987241 | HCID 56987241 | — |
Reaction Steps
A solution of thionyl chloride (530 μl, 7.27mmol) in THF (3 ml) was added to 4-methoxybenzyl (RS)-2-hydroxy-2-[(3S, 4R)-4-[3-oxo-3-[(S)-tetrahydrofuran-2-yl]propyl]-3-phthalimidoazetidin-2-on-1-yl]acetate (2.59 g, 4.84 mmol) and 2,6-lutidine (850 μl, 7.30 mmol) in THF (50 ml) at -20° C. After stirring for 1 h, the reaction mixture was filtered through a pad of celite, and the filtrate evaporated in vacuo. Toluene was added and re-evaporated to yield 4-methoxybenzyl (RS)-2-chloro-2-[(3S,4R)-4-[3-oxo-3-[(S)-tetrahydrofuran-2-yl]propyl]-3-phthalimidoazetidin-2-on-1-yl]acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716948 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-e660fe736afc4dfc9b1c59886adf5c41 |
| Source note | uspto-grants-1998_02 |