HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263594Generated: November 2, 2026
Water → 4-(beta-D-glucopyranos-1-yl)-2-(4-hydroxybenzyl)-benzonitrile
https://huagongshe.com/reaction/2263594
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-chloro-2-(4-acetoxy-benzyl)-4-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos-1-yl)-benzene | HCID 86608492 | — |
| Catalyst | Nickel(II) bromide | HCID 278492 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 4-(beta-D-glucopyranos-1-yl)-2-(4-hydroxybenzyl)-benzonitrile | HCID 86610215 | — |
Reaction Steps
A mixture of 200 mg 1-chloro-2-(4-acetoxy-benzyl)-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranos-1-yl)-benzene, 35 mg sodium cyanide and 75 mg nickel bromide in 0.5 mL N-methyl-2-pyrrolidinone is heated in a microwave oven at 220° C. for 15 min. After cooling to room temperature, water is added and the resultant mixture is extracted with ethyl acetate. After drying over sodium sulfate and evaporation of the solvent, the residue is dissolved in 3 mL methanol. 3 mL of 4 M aqueous potassium hydroxide solution is added and the reaction solution is stirred at ambient temperature for 3 h. The solution is neutralized with 1 M hydrochloric acid and the methanol is evaporated. The residue is extracted with ethylacetate, the combined extracts are dried over sodium sulfate and the solvent is removed under reduced pressure. The residue is purified by HPLC on reversed phase (YMC C18; water/acetonitrile 95:5->1:99).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851602B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-b48c8b5c50254c30b52a9b283b54300d |
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| Source note | uspto-grants-2010_12 |
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