HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(4-Bromo-butyl)-2-(4-fluoro-benzenesulfonyl)-N-trityloxy-acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | N-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide | HCID 86619940 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-Bromo-butyl)-2-(4-fluoro-benzenesulfonyl)-N-trityloxy-acetamide | HCID 86619941 | — |
Reaction Steps
N-(4-Bromo-butyl)-2-(4-fluoro-phenylsulfanyl)-N-trityloxy-acetamide from step D (105.2 mg, 0.182 mmol) and mCPBA (max. 77%, 0.21 g) in CH2Cl2 was stirred at room temperature for 30 min. The reaction was diluted with CH2Cl2 and water. The organic layer was sequentially washed with saturated Na2CO3 solution, 10% aqueous Na2SO3 and saturated Na2CO3 solution again. The organic phase was then dried and concentrated under the reduced pressure and purified by a column chromatography (0˜30% EtOAc in hexane). MS: 632.0, (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803793B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-b058ba553a584688b7471061afec3f45 |
| Source note | uspto-grants-2010_09 |