Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177725Generated: October 31, 2026

Boron tribromide → Ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate

https://huagongshe.com/reaction/2177725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoateHCID 67107394—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoateHCID 6710819273.8%

Reaction Steps

Boron tribromide (1M solution in DCM, 5.85 ml) was added dropwise to a stirred, cooled solution of ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-methoxybenzoate (Intermediate 61, 2.3 g) in dry DCM (45 ml) at −70° C. The resultant mixture was stirred at −70° C. for 40 minutes, then allowed to warm to room temperature. It was stirred at room temperature for 2 hours then poured into sodium bicarbonate (saturated aqueous solution). The layers were separated and the aqueous layer was extracted with further DCM. The combined organic layers were washed with brine, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness to give ethyl 6-(benzenesulphonylmethyl)-3-bromo-2-hydroxybenzoate (1.64 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-9b388b3b5dff40f0b2e05f1f08aa39c7
Source noteuspto-grants-2015_06