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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283477Generated: October 23, 2026

Acetic Anhydride → Acetate

https://huagongshe.com/en/reaction/1283477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPerchloric AcidHCID 24247—
ReactantSodium BicarbonateHCID 516892—
Reactant13-methyl-17alpha-ethynyl-3-methoxygona-2,5(10)-dien-17-OlHCID 86733826—
SolventEthyl AcetateHCID 8857—
ProductAcetateHCID 175—
ProductNorethindroneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03975412
Source datasetuspto-grants-1976_08
ORD IDord-4f3638211e3c4776a14f79af607aac78
Source noteuspto-grants-1976_08