HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580283Generated: October 30, 2026
Bromine → Dimethyl 3-bromothieno-[2,3-b]pyridine-5,6-dicarboxylate
https://huagongshe.com/reaction/580283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Dimethyl thieno[2,3-b]pyridine-5,6-dicarboxylate | HCID 13729652 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Dimethyl 3-bromothieno-[2,3-b]pyridine-5,6-dicarboxylate | HCID 13752488 | — |
Reaction Steps
Bromine (0.33, 0.00206 mol) in acetic acid (8 mL) is added to a stirred solution of dimethylthieno[2,3-b]pyridine-5,6-dicarboxylate (0.5 g, 0.00187 mol) in acetic acid containing sodium acetate (0.31 g, 0.00377 mol) at 40° C. The reaction mixture is heated at 75° C. for 18 hours. Evaluation of the mixture by tlc (silica gel) indicated incomplete reaction. Additional bromine (0.33 g) in acetic acid and sodium acetate (0.31 g) is added and heating at 75° C. continued for six hours. The reaction mixture is diluted with water and extracted into ethyl acetate. The separated organic layer is dried over anhydrous MgSO4, filtered, and the filtrate concentrated to an oil which solidifies on standing. Crystallization of the crude product from ethyl acetate-hexanes yields the dimethyl 3-bromothieno[2,3-b]pyridine-5,6-dicarboxylate as white needles mp 86°-87.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04752323 |
|---|
| Source dataset | uspto-grants-1988_06 |
|---|
| ORD ID | ord-68df54d6f2cc49f6bdabdcf66fd4bb94 |
|---|
| Source note | uspto-grants-1988_06 |
|---|