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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196835Generated: October 31, 2026

Acetylene → HCID 86745850, compound

https://huagongshe.com/reaction/1196835

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 54148456HCID 54148456—
ReactantHCID 178418443HCID 178418443—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86745850HCID 86745850—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 20 ml of dry tetrahydrofuran at 0° C. is added 0.75 ml of ethylmagnesium bromide (3 molar in ethyl ether) and through this solution is passed a stream of acetylene gas. After 30 min, 0.50 of ethylmagnesium bromide was added, followed after 30 min by another 0.50 ml of ethylmagnesium bromide. Acetylene gas is passed through the mixture all the time, and is continued for another 2 hr after the last addition. To the Grignard reagent is added dropwise 0.160 g of 5α-estr-2-en-17-one, Compound 6, dissolved in 5 ml of dry tetrahydrofuran. The combined reaction mixture is stirred at 0° C. for 2 hr, and then at room temperature for 16 hr. To the reaction mixture is added dropwise saturated ammonium chloride solution, water (30 ml) and ether (30 ml). The organic phase is separated, and the water phase is extracted once more with 12 ml of ether. The combined organic phase is washed twice with sodium chloride solution and dried over sodium sulfate. Evaporation of the solvent gave a brownish oil, which was purified on a silica gel column to give 0.087 g of Compound Ia, mp 107.5°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116830
Source datasetuspto-grants-1992_05
ORD IDord-e022dbc83e1a4df98d170e9a05e9791b
Source noteuspto-grants-1992_05