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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889281Generated: October 29, 2026

Boron tribromide → HCID 17747408, compound

https://huagongshe.com/reaction/889281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 68430767HCID 68430767—
SolventDichloromethaneHCID 6344—
ProductHCID 17747408HCID 17747408—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-(3,6-bis-benzyloxy-7-bromo-1-fluoronaphthalen-2-yl)-1,1-dioxo-[1,2,5]thiadiazolidin-3-one (232 mg, 0.406 mmol) in CH2Cl2 (3 mL) at 0° C. under nitrogen is added BBr3 (0.731 mL, 0.731 mmol). The reaction is stirred at 0° C. for 5 min then the mixture is quenched with 1N HCl (50 mL) and is extracted 3 times with EtOAc, dried over Na2SO4 and washed with brine. The organic layer is concentrated under reduced pressure and purified on reverse phase HPLC using a gradient of 10-20% MeCN/water (0.1% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08252820B2
Source datasetuspto-grants-2012_08
ORD IDord-39f44cdec07b44f696a9be502efa5dab
Source noteuspto-grants-2012_08