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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Phenyl-1,3-dioxane-5,5-diyl)bis(methylene) bis(4-methylbenzenesulfonate) | HCID 12458135 | — |
| Reactant | di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate | HCID 70957078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Di-tert-butyl (4S)-N-(tert-butoxvcarbonyl)-4-[4-({2-phenyl-5-[(tosyloxy)methyl]-1,3-dioxan-5-yl}methoxy)benzyl]-L-glutamate | HCID 89136260 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238631B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-0babea73b7054cd5b2eb3c64b5aaa7a9 |
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| Source note | uspto-grants-2016_01 |
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