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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263720Generated: November 2, 2026

Acetyl chloride → HCID 54371506, compound

https://huagongshe.com/reaction/263720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 54478735HCID 54478735—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 54371506HCID 5437150662.1%

Reaction Steps

Triethylamine (2 mL) was added to a solution of 6-methyl-N4 -(2-phenylethyl)-N2,N2 -bis(phenylmethyl)-pyridine-2,3,4-triamine (6 g, 14.2 mmole) in methylene chloride (50 mL). Acetyl chloride (1.1 mL, 15.5 mmole) was slowly added to the reaction mixture which was then heated on a steam bath for about 1 hour. The reaction mixture was stirred at ambient temperature overnight then diluted with water and methylene chloride. The organic phase was separated, washed with water, dried over magnesium sulfate and then concentrated under vacuum to provide a light green solid. This solid was slurried with ethyl acetate/hexane then recrystallized from ethyl acetate/hexane to provide 4.1 g of a white solid. A small portion (0.8 g) was purified by silica gel column chromatography to provide the desired compound as a white solid, m.p. 152°-153° C. Analysis: Calculated for C30H32N4O: % C, 77.56; % H, 6.94; % N, 12.06; Found: % C, 77.61; % H, 6.89: % N, 12.05.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05644063
Source datasetuspto-grants-1997_07
ORD IDord-a885bbc18e5444ccaea820093de3b058
Source noteuspto-grants-1997_07