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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071628Generated: November 3, 2026

Ammonium Chloride → HCID 22393742, compound

https://huagongshe.com/reaction/1071628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant3-(1,3-dioxolan-2-yl)thiophene-2-carbaldehydeHCID 11506572—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22393742HCID 2239374236.6%

Reaction Steps

20 ml of a THF solution of 4.49 g (40.0 mmol) of potassium tert-butoxide was cooled to −45 to −30° C., and 20 ml of a THF solution of 3.90 g (20.0 mmol) of TOSmic and 20 ml of a THF solution of 3.68 g (20.0 mmol) of 3-(1,3-dioxolan-2-yl)-2-thiophenecarboaldehyde were successively added thereto. After 40 minutes, 60 ml of methanol was added at −15° C. After heating under reflux for 15 minutes, an aqueous saturated ammonium chloride was added, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, to give a crude product. The crude product was subjected to Cromatorex NH silica gel (ethyl acetate:hexane=1:4), to give 1.43 g (7.32 mmol, 36.6%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906072B1
Source datasetuspto-grants-2005_06
ORD IDord-459621fcff294c72b0f35829aa2ccfcb
Source noteuspto-grants-2005_06