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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470628Generated: October 29, 2026

Boron tribromide → HCID 136413217, compound

https://huagongshe.com/reaction/470628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 67395995HCID 67395995—
SolventDichloromethaneHCID 6344—
ProductHCID 136413217HCID 136413217—

Reaction Steps

Boron tribromide (0.056 mL, 0,595 mmol) was added drop wise to a cooled solution of 1-benzyl-4-{5-[2-(3,4-dimethoxy-phenyl)-vinyl]-[1,2,4]oxadiazol-3-ylmethyl}-piperidine (compound of Example 30; 0.05 g, 0.12 mol) in dichloromethane (3 mL) at −78° C. The reaction mixture was warmed to room temperature and stirred for 6 h. The reaction mixture was quenched with methanol (2 mL) and the organic solvent was evaporated. The residue was suspended in methanolic ammonia (2 mL) and the undissolved solid was filtered. The filtrate was evaporated to obtain a crude product, which was purified by column chromatography (silica gel, 3% methanol in chloroform) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629277B2
Source datasetuspto-grants-2014_01
ORD IDord-eacf4603207c473896b3fa49751fe063
Source noteuspto-grants-2014_01