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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368031Generated: October 30, 2026

Tetrahydrofuran → HCID 86758993, compound

https://huagongshe.com/reaction/1368031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantCarbon tetrabromideHCID 11205—
ReactantHCID 86758994HCID 86758994—
ProductHCID 86758993HCID 86758993—

Reaction Steps

To a solution of 5-tertbutyloxy-carbonylamino-2-hydroxy-benzoic acid (20 g, 85.7 mmoles) in tetrahydrofuran (200 ml) triphenylphosphine (44.9 g, 171 mmoles) and lastly carbon tetrabromide (56.7 g, 171 mmoles) are added. The reaction mixture is left under stirring at room temperature for 24 hours and then evaporated under vacuum. The obtained residue is purified by silica gel column chromatography (eluent: n.-hexane/ethyl acetate 8/2 vol./vol.), monitoring the content of the collected fractions by chromatography on thin layer. The product is obtained by collecting the head fractions, after elution from the column of the CBr4 reactive used in the synthesis. The fractions are collected and dried. A white solid (21.16 mg) having m.p. 108°-111° C. is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573252B1
Source datasetuspto-grants-2003_06
ORD IDord-2e2bf571b7134d4e8bec2629607f0467
Source noteuspto-grants-2003_06