Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072673Generated: November 1, 2026

Acetyl chloride → HCID 22388588, compound

https://huagongshe.com/reaction/1072673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantHCID 10132502HCID 10132502—
SolventDichloromethaneHCID 6344—
ProductHCID 22388588HCID 22388588189.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of {2-[4-(3-Aminophenyl)phenoxy]propyl}[(methylethyl)sulfonyl]amine (125 mg, 0.3587 mmol, prepared in example 3) in methylene chloride (2.5 mL) in a 10 mL round-bottomed flask, in an ice bath, fitted with a thermometer, and under a nitrogen system was added triethylamine (0.125 mL, 0.8968 mmol). The mixture was cooled to 0° C. and acetyl chloride 0.04 mL, 0.5381 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 265 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 (104 mg, 74%) as a slow crystallizing foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911476B2
Source datasetuspto-grants-2005_06
ORD IDord-67760abd547143d891174b4db4ba1091
Source noteuspto-grants-2005_06