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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 984962Generated: October 31, 2026

Tetrahydrofuran → HCID 178520841, compound

https://huagongshe.com/reaction/984962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCarbon tetrabromideHCID 11205—
ReactantHCID 178520840HCID 178520840—
ProductHCID 178520841HCID 178520841—

Reaction Steps

To a solution of N-nicotinoyl-β-alanyl-(L)-histidine (9.9 g, 30.1 mmoles) in tetrahydrofuran (200 ml) triphenylphosphine (23.7 g, 90.3 mmoles) and carbon tetrabromide (28.85 g, 90.3 moles) are added under stirring. The reaction mixture is left under stirring at room temperature for 24 hours. Lastly the solvent is removed by evaporation at reduced pressure. The obtained crude product is purified by chromatography on silica gel column eluting with n-hexane/ethyle acetate 1/1. N-nicotinoyl-β-alanyl-(L)-histidine 4-bromobutyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06869974B1
Source datasetuspto-grants-2005_03
ORD IDord-0743f6c9942c45bd86eb924f0dd7b72d
Source noteuspto-grants-2005_03