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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611407Generated: November 1, 2026

Tetrahydrofuran → HCID 178520232, compound

https://huagongshe.com/reaction/1611407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCarbon tetrabromideHCID 11205—
ReactantHCID 178520231HCID 178520231—
ProductHCID 178520232HCID 178520232—

Reaction Steps

To a solution of [2-[(2,6-dichlorophenyl)amino]benzeneacetyloxy](L)-histidine (5 g, 11,54 mmoles) in tetrahydrofuran (100 ml) triphenylphosphine (9.08 g, 34.62 mmoles) and carbon tetrabromide (11.48 g, 34.62 mmoles) are added under stirring. The reaction mixture is left at room temperature for 24 hours, then the solvent is removed by evaporation at reduced pressure. The obtained crude product is purified by chromatography on silica gel eluting with n-hexane/ethyl acetate 1/1. (S)-[2-[(2,6-dichlorophenyl)amino]benzeneacetyloxy](L)-histidine 4-bromobutyl ester is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06987120B1
Source datasetuspto-grants-2006_01
ORD IDord-c955c6316284407a86577faf8bde215e
Source noteuspto-grants-2006_01