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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072674Generated: November 2, 2026

Triethylamine → HCID 22388583, compound

https://huagongshe.com/reaction/1072674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
ReactantHCID 10132502HCID 10132502—
SolventDichloromethaneHCID 6344—
ProductHCID 22388583HCID 22388583160.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of {2-[4-(3-aminophenyl)phenoxy]propyl}[(methylethyl)sulfonyl]amine (145 mg, 0.416 mmol, prepared in example 3) dissolved in methylene chloride (2.8 mL, anhydrous), was added triethylamine (0.15 mL, 1.04 mmol) under a nitrogen system. The mixture was cooled to 0° C. and isobutyryl chloride (0.13 mL, 1.25 mmol) was added by syringe. The mixture was allowed to warm to room temperature, and stirred overnight, under a nitrogen system. The reaction was quenched with excess water, and the organic layer was dried with anhydrous sodium sulfate, filtered, and concentrated under reduced vacuum, yielding 280 mg viscous oil. Purification was conducted using a Chromatotron®, on a 4000 μm rotor and eluting with a 1:1 hexane:ethyl acetate solvent system, yielding the title compound (136 mg, 78%) as a slow crystallizing foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911476B2
Source datasetuspto-grants-2005_06
ORD IDord-be1ccf8ae0e4424a9718b8627447858e
Source noteuspto-grants-2005_06