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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224038Generated: October 31, 2026

Tetrahydrofuran → HCID 178520841, compound

https://huagongshe.com/reaction/2224038

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 mmoles) 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/ethyl acetate 1/1. N-nicotinoyl-β-alanyl-(L)-histidine 4-bromobutyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378412B2
Source datasetuspto-grants-2008_05
ORD IDord-81ca109d78ba4b56ad7e4a3d05ed570c
Source noteuspto-grants-2008_05