HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(1'-Carboxy-1'-chloromethyl)-4-tritylthio-2-azetidinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1-(1'-Carboxy-1'-hydroxymethyl)-4-tritylthio-2-azetidinone | HCID 12780162 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(1'-Carboxy-1'-chloromethyl)-4-tritylthio-2-azetidinone | HCID 13909723 | — |
Reaction Steps
A cooled (ice bath) solution of the triethylamine salt of 1-(1'-carboxy-1'-hydroxymethyl)-4-tritylthio-2-azetidinone (1.04 g, 2.0 mmol) in methylene chloride (5 ml) was treated dropwise, under N2, with thionyl chloride (0.16 ml, 2.2 mmol) in methylene chloride (2 ml). The solution was stirred at room temperature for 20 min and concentrated. The residue was diluted with benzene and filtered over a Celite/charcoal bed. The filtrate was evaporated in vacuo to give 870 mg (quantitative) of the title compound as an amorphous solid. It was used in the next step without further purification. irνmax : 1775 cm-1 ; 1Hmr (CDCl3) δ: 9.22 (1H, bs), 7.27 (15H, m), 5.3 and 5.2 (1H, 2d, J=2 Hz), 4.6 (1H, m) and 2.8 ppm (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04378314 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-1f32561de5f643ce9001bbcb08ecad94 |
| Source note | uspto-grants-1983_03 |