HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-bromo-4H,5H,6H,7H-thieno(2,3-c)pyridine hydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4,5,6,7-Tetrahydrothieno(2,3-c)pyridine--hydrogen chloride (1/1) | HCID 25067333 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-bromo-4H,5H,6H,7H-thieno(2,3-c)pyridine hydrobromide | HCID 67027680 | 176.8% |
Reaction Steps
A solution of bromine (139 mg, 0.87 mmol) in acetic acid (0.5 mL) was added to a solution of 4,5,6,7-tetrahydrothieno[2,3-c]pyridine hydrochloride (150 mg, 0.85 mmol) in acetic acid (3 mL) and the mixture left to stir at ambient temperature for 1.5 h. The resultant precipitate was collected by filtration, washed with diethyl ether and left to air dry to afford the title compound as an off-white solid (230 mg, 90%). NMR (DMSO-D6, 300 MHz): 9.19 (s, 2H), 7.09 (s, 1H), 4.29-4.26 (m, 2H), 2.86-2.78 (m, 2H), 2.52-2.48 (m, 2H). LCMS (Method B): RT=1.65 min, M+H+=218/220.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09216980B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-4a407b8b3ecf45a5bfea946ececea87b |
| Source note | uspto-grants-2015_12 |