HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-[4-Hydroxy-5-(4-fluorophenoxy)pentyl]-methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 7-{N-[4-hydroxy-5-(4-fluorophenoxy)pentyl]methanesulfonamido}heptanoate | HCID 21401586 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-[4-Hydroxy-5-(4-fluorophenoxy)pentyl]-methanesulfonamide | HCID 86735163 | — |
Reaction Steps
A solution composed of ethyl 7-{N-[4-hydroxy-5-(4-fluorophenoxy)pentyl]methanesulfonamido}heptanoate (4.7 g., 0.11 mole), sodium hydroxide (1.0 g.), water (13 ml.) and ethanol (130 ml.) is kept at room temperature for 20 hours. Most of the solvent is removed in vacuo, water (150 ml.) is added and the solution extracted with ether (100 ml.). The aqueous layer is acidified (hydrochloric acid) and extracted with ethyl acetate (2 × 100 ml.). The organic layer is dried over sodium sulfate then concentrated in vacuo to obtain the subject compound. The yield is 3.7 g. (84%) of heavy oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055596 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-8aea0f1d361d4030aa76e40050d27a5d |
| Source note | uspto-grants-1977_10 |