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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591285Generated: October 30, 2026

Potassium Carbonate → Di-tert-butyl (4S)-N-(tert-butoxvcarbonyl)-4-[4-({2-phenyl-5-[(tosyloxy)methyl]-1,3-dioxan-5-yl}methoxy)benzyl]-L-glutamate

https://huagongshe.com/reaction/591285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Phenyl-1,3-dioxane-5,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate)HCID 12458135—
Reactantdi-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamateHCID 70957078—
SolventDimethylformamideHCID 6228—
ProductDi-tert-butyl (4S)-N-(tert-butoxvcarbonyl)-4-[4-({2-phenyl-5-[(tosyloxy)methyl]-1,3-dioxan-5-yl}methoxy)benzyl]-L-glutamateHCID 89136260—

Reaction Conditions

Temperature100 °C

Reaction Steps

To 466 mg (1.0 mmol) of di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate in 12 mL N,N-dimethylformamide were added 138 mg (1.0 mmol) of potassium carbonate and 533 mg (1.0 mmol) of (2-phenyl-1,3-dioxane-5,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate) (Heterocycles 34. (1992), 739), and the resulting suspension was heated for 2 h at 100° C. in a microwave oven. The reaction mixture was then filtered, the solvent evaporated and the residue was taken up in ethyl acetate and water. The organic phase was separated off, washed with water until neutral, dried over sodium sulfate and filtered, and the filtrate was concentrated in vacuo. The residue was chromatographed on silica gel using a dichloromethane/ethyl acetate gradient, and the appropriate fractions were combined and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238631B2
Source datasetuspto-grants-2016_01
ORD IDord-0babea73b7054cd5b2eb3c64b5aaa7a9
Source noteuspto-grants-2016_01