HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76314Generated: October 29, 2026
Boron tribromide → 2,6-Dibromo-benzo[1,2-b:4,5-b']dithiophene-4,8-diol
https://huagongshe.com/reaction/76314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 86696622 | HCID 86696622 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dibromo-benzo[1,2-b:4,5-b']dithiophene-4,8-diol | HCID 86696621 | — |
Reaction Steps
2,6-Dibromo-4,8-dimethoxy-benzo[1,2-b:4,5-b′]dithiophene (500 mg, 1.22 mmol., 1.00 equiv.) and dichloromethane (12 mL) were added to a 50 mL schlenk flask. The mixture was cooled to −78° C. and boron tribromide was added (1.0 M solution in dichloromethane, 2.5 mL, 2.5 mmol., 2.1 equiv.) slowly. The mixture was stirred for 15 minutes at −78° C. before replacing the dry/ice acetone bath with an ice/water bath. The reaction mixture was left to warm to room temperature while stirring for 16 hours before cooling to 0° C. Water (dropwise at first, 150 mL total) and additional dichloromethane (50 mL) were added. The dichloromethane was removed on the rotary evaporator and the solid was collected by filtration. The solid was washed with water (25 mL) and dichloromethane (25 ml) to give a pale blue/green crude solid to be dried under vacuum and used in the next step without additional purification (287 mg). 1H NMR (400 MHz, CDCl3) δ 10.13 (s, 2H), 7.71 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08835598B2 |
|---|
| Source dataset | uspto-grants-2014_09 |
|---|
| ORD ID | ord-1a80e4f6593f43128f1947814285a427 |
|---|
| Source note | uspto-grants-2014_09 |
|---|