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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638817Generated: November 1, 2026

Acetic Acid → HCID 14676180, compound

https://huagongshe.com/reaction/1638817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantHCID 14676181HCID 14676181—
SolventDiethyl EtherHCID 3283—
ProductHCID 14676180HCID 1467618083.4%

Reaction Steps

A mixture of 1-(3-benzyloxy-2-methoxy-6,7-dihydro-5H-benzocyclohepten-8-ylcarbonyl)-4-(3,4,5-trimethoxybenzoyl)piperazine (1.7 g), a 30% acetic acid solution of hydrobromic acid (6 ml) and acetic acid (12 ml) is stirred at room temperature for 40 minutes. To the reaction mixture is added ether (100 ml), and the resulting precipitates are collected by filtration. To the precipitates are added ethyl acetate and water. The mixture is shaken, then the organic layer is separated. The organic layer is washed with an aqueous solution of sodium hydrogencarbonate, and water, and dried, followed by distilling off the solvent under reduced pressure. The residue is purified by silica gel column chromatography (eluent, hexane:ethyl acetate:acetone:methylene chloride=1:1:1:1) to give 1-(3-hydroxy-2-methoxy-6,7-dihydro-5H-benzocyclohepten-8-ylcarbonyl)-4-(3,4,5-trimethoxybenzoyl)piperazine (1.2 g). Recrystallization of this product from ethyl acetate affords colorless crystals, m.p. 198°-199° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04880809
Source datasetuspto-grants-1989_11
ORD IDord-cbe8be8cf5484d518957ed9ad21f6c50
Source noteuspto-grants-1989_11