HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 5,6-Dihydro-4H-pyrrolo[3,4-d]thiazole Hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Phenol | HCID 996 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 5-(benzenesulfonyl)-4,6-dihydro-5H-pyrrolo[3,4-d]thiazole | HCID 18442806 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5,6-Dihydro-4H-pyrrolo[3,4-d]thiazole Hydrobromide | HCID 18442779 | — |
Reaction Steps
A mixture of 5-(benzenesulfonyl)-4,6-dihydro-5H-pyrrolo[3,4-d]thiazole (800 mg), phenol (800 μl) and 47% hydrobromic acid (5.00 ml) was heated under reflux for 2 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and water were added to conduct liquid separation. The resultant water layer was concentrated under reduced pressure. Ethyl acetate was added to the residue, colorless powder deposited was collected by filtration to obtain the title compound (521 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07935824B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-9d2b7fda0ab04235b69314818d1d2e51 |
| Source note | uspto-grants-2011_05 |