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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1059107Generated: November 2, 2026

Water → HCID 18670800, compound

https://huagongshe.com/reaction/1059107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHCID 18670784HCID 18670784—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthyl 3-(naphthalen-1-yl)prop-2-enoateHCID 53428571—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18670800HCID 1867080066.1%

Reaction Steps

3-ethoxycarbonyl-5-methyl-4-(naphthalen-1-yl)-1H-pyrrole 4.3 g(18.9 mmol) of 3-(naphthalen-1-yl)-acrylic acid ethylester prepared in Preparation 6-1) and 3.95 g(18.9 mmol) of α-methyltosylmethylisocyanide disclosed in A. M. van Leusen, et al., Tetrahedron Letter, 1975, 40, 3487 were dissolved in 100 ml of tetrahydrofuran. 2.55 g(22.7 mmol) of potassium t-butoxide dissolved in 100 ml of tetrahydrofuran was slowly added thereto, which was then refluxed for 30 minutes. To the reaction solution was added 100 ml of water to stop the reaction and the solvent was removed under reduced pressure. The residue was extracted with diethylether, washed with saturated sodium chloride solution and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue was subjected to silica gel column chromatography using a solvent mixture of ethyl acetate/n-hexane(1/3, v/v) as an eluent to give 3.50 g(12.5 mmol, Yield 66%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06518429B2
Source datasetuspto-grants-2003_02
ORD IDord-0bf3e081ee7f49e493a1ec9fd7b75ab5
Source noteuspto-grants-2003_02