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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387315Generated: October 30, 2026

Water → HCID 18670784, compound

https://huagongshe.com/reaction/1387315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-(1-Isocyanoethanesulfonyl)-4-methylbenzeneHCID 11052885—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantEthyl 3-(naphthalen-1-yl)prop-2-enoateHCID 53428571—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18670784HCID 1867078466%

Reaction Steps

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 dissoved 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 numberUS06268363B1
Source datasetuspto-grants-2001_07
ORD IDord-b3c895e146c64aa0bc72c239c6ba4305
Source noteuspto-grants-2001_07