HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21401589, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 7-[N-(4,5-epoxypentyl)methanesulfonamido]heptanoate | HCID 21401575 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21401589 | HCID 21401589 | — |
Reaction Steps
To a solution of ethyl 7-[N-(4,5-epoxypentyl)- methanesulfonamido]heptanoate (7.0g., 0.02 mole) in ethanol (150 ml.) is added sodium hydroxide (1.84 g., 0.046 mole) dissolved in water (15 ml.). This solution is stirred at room temperature for 18 hours, then concentrated to one-half volume under reduced pressure. Water (150 ml.) is added and this aqueous solution is extracted with ether (2 × 100 ml.). The aqueous layer is then acidified (dilute hydrochloric acid) and extracted with ethyl acetate (2 × 150 ml.). The organic phase is washed with brine, dried over sodium sulfate, then evaporated in vacuo. The yield of subject compound is 4.0 g. (54%) of pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055596 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-4426bf2078cb4265afad9b7000ddc2eb |
| Source note | uspto-grants-1977_10 |