HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-Chloro-2-(4-methoxymethylethynyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-chloro-4-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranos1-yl)-2-(4-methoxymethylethynyl-benzyl)-benzene | HCID 86605977 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Chloro-2-(4-methoxymethylethynyl-benzyl)-4-(beta-D-glucopyranos-1-yl)-benzene | HCID 86605983 | — |
Reaction Steps
To a solution of 0.11 g 1-chloro-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranos1-yl)-2-(4-methoxymethylethynyl-benzyl)-benzene in 2 mL methanol is added 0.85 mL of 1 M aqueous potassium hydroxide solution. The solution is stirred for 1 h at ambient temperature and then diluted with ethyl acetate. The resulting solution is washed with brine and dried over sodium sulfate. The solvent is evaporated and the residue is filtered through silica gel (dichloromethane/methanol 9:1->2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687469B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-69b0b11e5e594d339ba81144c7d66dc6 |
| Source note | uspto-grants-2010_03 |