HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → Ethyl 9-ethylenedioxy-15-hydroxy-15-methylprostanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | Ethyl 9-ethylenedioxy-15-oxo-prostanoate | HCID 68123704 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 9-ethylenedioxy-15-hydroxy-15-methylprostanoate | HCID 68124131 | — |
Reaction Steps
To a Grignard solution prepared from 207 mg. of magnesium and 1.3 g. of methyl iodide in 10 ml. of ether under nitrogen atmosphere is added a solution of 1.77 g. of ethyl 9-ethylenedioxy-15-oxo-prostanoate (Example 56) in 10 ml. of ether and the resulting mixture is stirred at room temperature for 18 hours. Saturated ammonium chloride (20 ml.) is added followed by 10 ml. of water and 50 ml. of ether. The ethereal solution is washed with saturated sodium chloride solution, dried with anhydrous magnesium sulfate and taken to dryness to give 1.77 g. (94%) of viscous oil; λ max. 2.94 (hydroxyl group) and 5.77 μ (carbonyl group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017534 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-0024128f7db944d182b0b1ef62a51cda |
| Source note | uspto-grants-1977_04 |