Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2381188Generated: November 3, 2026

Boron tribromide → HCID 51001654, compound

https://huagongshe.com/reaction/2381188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 51001655HCID 51001655—
SolventDichloromethaneHCID 6344—
ProductHCID 51001654HCID 5100165471.5%

Reaction Steps

1-(Toluene-4-sulfonyl)-piperidine-4-carboxylic acid [4-((R)-3-methoxy-1-trifluoromethyl-propoxy)-phenyl]-amide (0.105 g), product of example 59), in methylene chloride (2 ml) was treated at RT and under an argon atmosphere with BBr3 (0.5 molar, 1 ml) for 2 h. The mixture was then partitioned between diethyl ether and aqueous 1N HCL, the layers were separated, the organic layer was dried over sodium sulphate, and evaporated off to give the desired 1-(toluene-4-sulfonyl)-piperidine-4-carboxylic acid [4-((R)-3-hydroxy-1-trifluoromethyl-propoxy)-phenyl]-amide (0.073 g) as light brown crystalline solid. MS (ESI): 501.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258158B2
Source datasetuspto-grants-2012_09
ORD IDord-6511b44a98774b77a45711610c98b2bd
Source noteuspto-grants-2012_09