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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367319Generated: October 30, 2026

Ammonium Chloride → HCID 178431197, compound

https://huagongshe.com/reaction/367319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178475395HCID 178475395—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178431197HCID 17843119725.1%

Reaction Steps

Under a nitrogen atmosphere, 2.0 g of 1-{4-[(5-acetoxy-4,6-di-t-butyl-2-methyl-2,3-dihydrobenzofuran-2-yl)methoxy]benzylideneamino}guanidine was dissolved in 100 ml of tetrahydrofuran, and 10 ml of n-butyl lithium (1.6 M in n-hexane) was added and the mixture was stirred at room temperature for 30 minutes. After reaction, the reaction solution was combined with a saturated aqueous ammonium chloride solution and extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and then concentrated. The concentrate was purified by silica gel column chromatography eluting with chloroform containing 10% methanol to give 0.46 g of 1-{4-[(4,6-di-t-butyl-5-hydroxy-2-methyl-2,3-dihydrobenzofuran-2-yl)methoxy]benzylideneamino}guanidine as a pale yellow solid (yield 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133279
Source datasetuspto-grants-2000_10
ORD IDord-502e1f88ca0a4ec5a6c4c26b2e52a258
Source noteuspto-grants-2000_10