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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268115Generated: October 31, 2026

Decanoyl chloride → HCID 12041318, compound

https://huagongshe.com/reaction/1268115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDecanoyl chlorideHCID 66982—
ReactantHCID 12041317HCID 12041317—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12041318HCID 1204131898.2%

Reaction Steps

In a stream of nitrogen and at 0° C., 0.16 ml (0.80 mmol) of decanoyl chloride was added to an anhydrous tetrahydrofuran (10 ml) solution containing 300 mg (0.70 mmol) of 3-(4-nitrobenzyloxy)-N-(2-sulfamoylphenyl)benzamide produced in Reference Example 5 and 171 mg (1.40 mmol) of 4-dimethylaminopyridine, the mixture was stirred at room temperature for 1 hour and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with water, a potassium hydrgensulfate aqueous solution and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The resulting residue was purified by a silica gel column chromatography to obtain 400 mg (yield: 97.9%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555584B1
Source datasetuspto-grants-2003_04
ORD IDord-2376c1c2c9574017ae6f2609d19291ed
Source noteuspto-grants-2003_04