HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445340Generated: October 29, 2026
Potassium Carbonate → HCID 21961241, compound
https://huagongshe.com/reaction/1445340
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | alpha-D-Galactopyranosyl bromide, tetraacetate | HCID 102932 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-Benzyl-3-hydroxythiophene-2-carboxamide | HCID 54704139 | — |
| Catalyst | Benzyltributylammonium chloride | HCID 159952 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21961241 | HCID 21961241 | — |
Reaction Steps
1.12 g of N-benzyl-3-hydroxy-thiophene-2-carboxamide, 3.16 g of 4,5-diacetoxy-6-acetoxymethyl-2-bromo-tetrahydro-pyran-3-yl acetate, 3.30 g of potassium carbonate and 235 mg of benzyltributylammonium chloride were dissolved in 25 ml of dichloromethane, and 2.00 ml of water were added. The reaction mixture was stirred at 22° C. for 40 h. 50 ml of saturated sodium bicarbonate solution were added to the reaction mixture, which was extracted twice with 50 ml of dichloromethane each time. The combined organic phases were dried over magnesium sulfate and concentrated. The crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07666848B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-c766fa5d03854dc39496352efec61947 |
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| Source note | uspto-grants-2010_02 |
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