HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 14209149, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 54369044 | HCID 54369044 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14209149 | HCID 14209149 | 96.7% |
Reaction Steps
To a solution of 0.31 g (1 millimole) of ethyl [1-(2,4-dimethoxy-benzyl)-4-oxo-2-azetidinyl]-acetate and 4 ml of ethanol a solution of 0.04 g (1 millimole) of sodium hydroxide and 6 ml of water are added. The reaction mixture is stirred at room temperature for 2 hours. The solution is extracted three times with 3 ml of dichloromethane each. The aqueous layer is acidified with concentrated aqueous hydrochloric acid to pH 2 and extracted three times with 3 ml of dichloromethane each. The united organic layers are dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated. The residue is crystallized from benzene. Thus 0.27 g of the desired compound are obtained, yield: 88%, M.p.: 112° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04587049 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-ee76ee87ee8744208d54f8e3234bc2cf |
| Source note | uspto-grants-1986_05 |