HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine →
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Toluene-p-sulphonic anhydride | HCID 77773 | — |
| Reactant | 3-Thietan-1-ol | HCID 82532 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
Reaction Steps
A solution of thietan-3-ol (450 mg) and Et3N (1.3 ml) in chloroform (5 ml) was added dropwise to over 30 minutes to a solution of p-toluenesulfonic anhydride (1.63 g) in dichloromethane (10 ml) at −20° C. under argon atmosphere. After 2 hours, pyridine (0.8 ml) was added and the resulting mixture was stirred at room temperature for 2 days. The precipitated solid was collected by filtration (300 mg). 1H-NMR (DMSO, 400 MHz): 2.30 (s, 3H), 3.57 (t, 2H), 4.09 (t, 2H), 6.16 (q, 1H), 7.12 (d, 2H), 7.50 (d, 2H), 8.20 (t, 2H), 8.66 (t, 1H), 9.21 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006456B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-f6282334725840aa94460d01e1cd0494 |
| Source note | uspto-grants-2015_04 |