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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249641Generated: October 28, 2026

Hydrochloric Acid → HCID 68983961, compound

https://huagongshe.com/reaction/2249641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantMethanesulfonamideHCID 72879—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 57684398HCID 57684398—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68983961HCID 6898396194.5%

Reaction Steps

In 10 ml of tetrahydrofuran is dissolved 1.00 g of 3-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl]-propanoic acid, to which is added 0.52 g of 1,1′-carbonyldiimidazole at ambient temperature. The mixture thus obtained is heated under reflux for one hour with stirring. To the reaction mixture cooled to ambient temperature are added 0.22 g of methane-sulfonamide and 0.4 ml of 1,8-diazabicyclo[5.4.0]undec-7-ene, and the mixture thus obtained is stirred for 30 minutes at ambient temperature. The reaction mixture is added to a mixture of chloroform and water, pH is adjusted to 2 with 6 mol/L hydrochloric acid, and the organic layer is separated. The organic layer thus obtained is washed with water and saturated aqueous solution of sodium chloride successively and dried over anhydrous magnesium sulfate, and the solvent is distilled off under reduced pressure. The residue thus obtained is purified by silica gel column chromatography (eluent; hexane:ethyl acetate=2:1) to obtain 1.10 g of N-{3-[5-(2,4-diisobutoxybenzoyl)-2-isobutoxyphenyl]propanoyl}methanesulfonamide as a white-colored foaming product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314888B1
Source datasetuspto-grants-2008_01
ORD IDord-8e697479f02c4e989ffd2114f2164548
Source noteuspto-grants-2008_01