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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067180Generated: November 1, 2026

Boron tribromide → HCID 57725645, compound

https://huagongshe.com/reaction/2067180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 57725407HCID 57725407—
SolventDichloromethaneHCID 6344—
ProductHCID 57725645HCID 5772564572.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (S)—N-(1-cyclohexylethyl)-6-methoxybenzo[d]thiazol-2-amine (3.39 g, 10 mmol) in 30 mL of DCM was added 1 M boron tribromide in DCM (20 mL, 20 mmol) slowly at 0° C. The reaction solution was stirred at 0° C. for 20 min and then at room temperature for 2 hours. The reaction mixture was concentrated in vacuo and the residue was dissolved in EtOAc (400 mL) and water (90 mL) and stirred at room temperature for 10 min. To the mixture was added excess solid NaHCO3 until basic. Stirring was continued at room temperature for 1 hour. The separated aqueous layer was extracted with EtOAc (100 mL). The combined organic layers were washed water (50 mL), saturated NaCl solution (50 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure. Purification by silica gel column chromatography with EtOAc/hexanes (3/7) provided the title compound as a solid (2.0 grams). ES/MS m/z 277.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293769B2
Source datasetuspto-grants-2012_10
ORD IDord-231ee11dea714dc8b4cb07520a40f04b
Source noteuspto-grants-2012_10