HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 13-methyl-17alpha-ethynyl-3-methoxygona-2,5(10)-dien-17-Ol | HCID 86733826 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Acetate | HCID 175 | — |
| Product | Norethindrone | HCID 6230 | — |
Reaction Steps
Prepare a fresh solution of acetic anhydride (4.8 ml.) and 70% aqueous perchloric acid (0.01 ml.) in ethyl acetate (50 ml.) then add dl-13-methyl-17α-ethynyl-3-methoxygona-2,5(10)-dien- 17-Ol (0.5 g.) as a solid, swirl for 1.5 minutes then quench the reaction by adding saturated aqueous sodium bicarbonate solution. Wash the ethyl acetate layer with saturated bicarbonate, brine and dry over anhydrous sodium sulfate. Filter, evaporate in vacuo then add methanol with a trace of pyridine and let stand for 2 hours. Evaporate in vacuo, pump dry then treat the residue in ether with decolorizing charcoal. Filter, evaporate and crystallize the residue from methanol to obtain dl-13-methyl-17α-ethynyl-17-hydroxygon-4-en-3-one, acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03975412 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-4f3638211e3c4776a14f79af607aac78 |
| Source note | uspto-grants-1976_08 |