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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473393Generated: October 30, 2026

Boron tribromide → HCID 86687436, compound

https://huagongshe.com/reaction/1473393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 86687434HCID 86687434—
SolventDichloromethaneHCID 6344—
ProductHCID 86687436HCID 86687436—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-(benzylthio)-1-chloro-4-methoxyisoquinoline (Intermediate VVV; 0.400 g, 1.267 mmol) was dissolved in DCM (12.67 ml) and cooled to 0° C. Boron tribromide (0.487 ml, 5.06 mmol) was added and the reaction was stirred for 30 minutes, then warmed to room temperature and stirred overnight. The reaction was cooled to 0° C. and carefully quenched with saturated sodium bicarbonate solution. The reaction was diluted with ethyl acetate and the layers were separated. The aqueous layer was extracted with ethyl acetate, and the combined organic layers were dried with sodium sulfate, filtered, and concentrated to afford crude 6-(benzylthio)-1-chloroisoquinolin-4-ol as an orange solid. (ESI) 302.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012443B2
Source datasetuspto-grants-2015_04
ORD IDord-9fd106f93ee245a7b2164d2213ab4bfe
Source noteuspto-grants-2015_04