HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716322Generated: November 3, 2026
4-Methoxyphenol → 3-[4-(4-Methoxy-phenoxy)-benzenesulfonyl]-1-trityloxy-azepan-2-one
https://huagongshe.com/reaction/1716322
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxyphenol | HCID 9015 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(4-Fluoro-benzenesulfonyl)-1-trityloxy-azepan-2-one | HCID 68513693 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 3-[4-(4-Methoxy-phenoxy)-benzenesulfonyl]-1-trityloxy-azepan-2-one | HCID 68516340 | — |
Reaction Steps
A Mixture of 3-(4-fluoro-benzenesulfonyl)-1-trityloxy-azepan-2-one prepared from step F (18.9 mg, 0.0357 mmol), 4-methoxy-phenol (19.2 mg, 0.154 mmol) and K2CO3 (38.1 mg, 0.275 mmol) in anhydrous DMA (1.5 mL) was stirred and heated at 100° C. for overnight. The reaction mixture was diluted with EtOAc and washed sequentially with water and saturated NaCl solution. The organic phase was then dried over anhydrous Na2SO4 and concentrated under reduced pressure to gave a crude material, which was then purified by a column chromatography (0˜25% EtOAc in hexane). MS: 656.5 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803793B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-37e6fe15b55f43ab91300e09decc8e94 |
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| Source note | uspto-grants-2010_09 |
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