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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499731Generated: October 25, 2026

Ammonium Chloride → 3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-[5-(4-ethylphenyl)methyl-2-(2-trityloxyethyl)thiophen-3-yl]-tetrahydropyran-2-ol

https://huagongshe.com/reaction/499731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3,4,5-Tribenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-oneHCID 4585508—
Reactant3-Bromo-5-((4-ethylphenyl)methyl)-2-(2-trityloxyethyl)thiopheneHCID 68460416—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product3,4,5-Tris-benzyloxy-6-benzyloxymethyl-2-[5-(4-ethylphenyl)methyl-2-(2-trityloxyethyl)thiophen-3-yl]-tetrahydropyran-2-olHCID 8662663765%

Reaction Steps

Under a nitrogen stream, to a solution of 3-bromo-5-((4-ethylphenyl)methyl)-2-(2-trityloxyethyl)thiophene (1.45 g, 2.55 mmol) in anhydrous THF (40 ml), a hexane solution of n-butyllithium (1.6 M, 1.76 ml, 2.81 mmol) was added dropwise at −78° C. and the mixture was stirred for 15 minutes. To this solution was added a solution of 3,4,5-trisbenzyloxy-6-(benzyloxymethyl)tetrahydropyran-2-one (1.50 g, 2.81 mmol) in anhydrous THF (10 ml) dropwise at −78° C. and the resulting solution was stirred at the same temperature for 10 minutes. After addition of saturated aqueous ammonium chloride, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then evaporated under reduced pressure to remove the solvent. The resulting residue was purified by silica gel column chromatography (developing solution=ethyl acetate:n-hexane (1:20)) to give the titled compound (1.70 g, 65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767651B2
Source datasetuspto-grants-2010_08
ORD IDord-be7255b86c9e47069d6c76538c2b9a07
Source noteuspto-grants-2010_08