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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606273Generated: October 30, 2026

Diisopropylethylamine → HCID 11376023, compound

https://huagongshe.com/reaction/606273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-IsopropoxyanilineHCID 82112—
Reactant3,5-Dichloro-4-(2-chloro-4-nitrophenoxy)benzene-1-sulfonyl chlorideHCID 2774361—
SolventDichloromethaneHCID 6344—
ProductHCID 11376023HCID 1137602363%

Reaction Conditions

Temperature40 °C

Reaction Steps

To 100 mg of 3,5-Dichloro-4-(2-Chloro-4-Nitrophenoxy)Benzene-1-Sulfonyl Chloride (0.23 m.mol) was added 0.2 ml of DIEA, 5 ml of dichloromethane and 150 mg of 4-isopropoxyaniline. The mixture was maintained at 40° C. for 4 hours. The solvent was evaporated and the residue dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous Na2SO4 and the solvent evaporated. The residue as purified using radial silica-gel chromatography using 1:4 ethyl acetate:hexane as solvent. The purity of the product by LC/MS was 97.19%. M−1 (530) was seen in the mass spectrum. The yield of the product was 80.3 mg or 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915293B2
Source datasetuspto-grants-2011_03
ORD IDord-8dedc6aaf12146a6a4052dd271b8421d
Source noteuspto-grants-2011_03