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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940213Generated: November 1, 2026

Phenol → HCID 6918291, compound

https://huagongshe.com/reaction/1940213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 10334891HCID 10334891—
SolventAcetonitrileHCID 6342—
ProductHCID 6918291HCID 691829163%

Reaction Steps

A solution of 3-bromomethyl-2,2,4,6,7-pentamethyl-2,3-dihydro-1-benzofuran-5-ol (81 g, 270 mmol), phenol (26.75 g, 284 mmol) and N-methylpiperazine (28.47 g, 284 mmol) in acetonitrile (300 ml) is stirred at reflux temperature for 60 hrs. The precipitate that formed is collected, washed with acetonitrile and slurtied in 10% sodium bicarbonate solution. The product is extracted twice with ethyl acetate, and the extract is washed with water and brine, dried (sodium sulfate) and evaporated. The resulting solid is dissolved in ethanol (150 mL) and 2N hydrochloric acid (150 mL), and evaporated to near dryness. The resulting solid is recrystallized in ethanol/ethyl acetate to give after drying at 60° C. under 13 Pa and equilibration in a moist atmosphere for 24 hrs, 48.60 g (44%) of 2,2,4,6,7-pentamethyl-3-[(4-methylpiperazino)-methyl]-2,3-dihydro-1-benzofuran-5-ol dihydrochloride hydrate, mp=172°-3° C.(dec.). A second crop of 19.63 g of 2,2,4,6,7-pentamethyl-3-[(4-methylpiperazino)-methyl]-2,3-dihydro-1-benzofuran-5-ol (total yield 63%) could be obtained from the filtrate after purification of the free base by column chromatography on silica gel eluting with dichloromethane/methanol 9:1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698696
Source datasetuspto-grants-1997_12
ORD IDord-11bc0edce4c94e979569e4017c76b9f0
Source noteuspto-grants-1997_12