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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452311Generated: October 30, 2026

Boron tribromide → HCID 58362651, compound

https://huagongshe.com/reaction/452311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58362463HCID 58362463—
SolventDichloromethaneHCID 6344—
ProductHCID 58362651HCID 58362651—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a round bottomed flask equipped with a magnetic stir bar containing DCM (5 vol) is placed 4-((6-methoxybenzo[d]thiazol-2-yl)ethynyl)-N-methyl-2-nitroaniline (1 equiv). The reaction mixture is cooled to 0° C., BBr3 (5 equiv of 1M in DCM) is added dropwise and the reaction is stirred at RT for 8 hours. The reaction is neutralized with sat. NaHCO3, extracted into DCM (2×5 vol). The combined organic extracts are washed with water (5 vol), brine (5 vol), dried over MgSO4 and concentrated in vacuo. The residue is purified over silica gel using EtOAc:Hexanes (1:3) as an eluent to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08491869B2
Source datasetuspto-grants-2013_07
ORD IDord-74909d2f5c3046cb84888e83626370de
Source noteuspto-grants-2013_07