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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78392Generated: October 29, 2026

Boron tribromide → 2,6-Dibromo-benzo[1,2-b:4,5-b']dithiophene-4,8-diol

https://huagongshe.com/reaction/78392

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 numberUS08841409B2
Source datasetuspto-grants-2014_09
ORD IDord-0c39fe31202b48c3af65839b96b9783a
Source noteuspto-grants-2014_09