HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 2763195, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | tert-Butyl [(3S)-2-oxooxetan-3-yl]carbamate | HCID 2763194 | — |
| Product | HCID 2763195 | HCID 2763195 | 81% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a stirred mixture of 2 (1.34 mmol) and anhydrous p-toluenesulphonic acid (72 h under vacuum in the presence of P2O5) (1.43 mmol), kept at 0° C. under N2, trifluoroacetic acid (3 mL) was added dropwise in the course of 10 min. The solution was reacted under stirring at 0° C. for 15 min, allowed to reach room temperature, and concentrated at a temperature below 30° C. The oily residue was kept under vacuum for 1 h, and the resulting white solid triturated and washed with dry diethyl ether, then kept under vacuum for 24 h. Yield 81%. Mp and 1H NMR are in accordance with literature (Arnold, et al., 1988).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321743B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-8a443917c8764817a3893f8fe4a38ce2 |
| Source note | uspto-grants-2016_04 |