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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195825Generated: November 2, 2026

Diethyl Ether → beta-Ethenylidene-2-thiopeneethanamine

https://huagongshe.com/reaction/1195825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium HydroxideHCID 14923—
ReactantN,N-bis(trimethylsilyl)-4-methoxy-2-butynylamineHCID 13161121—
ReactantHCID 178418438HCID 178418438—
CatalystNickel DichlorideHCID 24385—
SolventEthyl AcetateHCID 8857—
ProductAmmonium HydroxideHCID 14923—
Productbeta-Ethenylidene-2-thiopeneethanamineHCID 1451811087%

Reaction Steps

NiCl2 (dppp) catalyst (170 mg; 3M %) was added to dry ether (30 ml) in a 100 ml 3-necked flask with mechanical stirrer, thermometer and nitrogen bubbler. III (2.47 g, 10.2 mM) was added via syringe with stirring and immediately thereafter 3M thienylmagnesium bromide (7 ml, 21 mM) was added via syringe. After stirring at room temperature for 20 hours the reaction was complete as shown by G C analysis. The silylated product was isolated by shaking with dilute NH4OH and extraction into ethylacetate (three times, each into 100 ml). After drying over K2CO3 and concentration, 2.68 g crude product was obtained. Purification and desilylation by flash chromatography (300 g silica gel, eluted with CHCl3, then CHCl3 :MeOH:conc. NH4OH 100:10:1) gave 1.22 g (87%) of the desired product as a light tan oil after drying under high vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112852
Source datasetuspto-grants-1992_05
ORD IDord-b6098608db7a4f1a9b8de21ce01d3dc0
Source noteuspto-grants-1992_05