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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514169Generated: October 30, 2026

Boron tribromide → HCID 136340575, compound

https://huagongshe.com/reaction/514169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 86662507HCID 86662507—
SolventDichloromethaneHCID 6344—
ProductHCID 136340575HCID 13634057516.5%

Reaction Steps

3.04 g of 5,5′-(2,5-bis(hexyloxy)-1,4-phenylene)bis(2-(3-(4-nitrophenoxy)phenyl)-1,3,4-oxadiazole) (3.6 mmol) prepared in Synthesis Example 9 was dissolved in 120 ml of dichloromethane at −78□, and 3.5 ml of boron tribromide (35.6 mmol) was added thereto, followed by slowly raising the temperature to 0□. Thereafter, the reaction was quenched by addition of methanol, followed by adding excess water. The resultant solution was neutralized with dichloromethane, filtered, and performing silica gel column chromatography (developed with trichloromethane) to yield 0.4 g of a product having Formula 38. 1H NMR (300 MHz, CDCl3) analytical results of the product were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09106057B2
Source datasetuspto-grants-2015_08
ORD IDord-65f2afd4d3ed46829c4443b98e1688fe
Source noteuspto-grants-2015_08