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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 86696622HCID 86696622—
SolventDichloromethaneHCID 6344—
Product2,6-Dibromo-benzo[1,2-b:4,5-b']dithiophene-4,8-diolHCID 86696621—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835598B2
Source datasetuspto-grants-2014_09
ORD IDord-1a80e4f6593f43128f1947814285a427
Source noteuspto-grants-2014_09