Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309281Generated: November 2, 2026

Sodium amide → 1,3,5-Tris[3-(3-tert-butyl-2-hydroxy-5-methylphenyl)propoxycarbonyl]benzene

https://huagongshe.com/reaction/2309281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium amideHCID 24533—
ReactantTrimethyl benzene-1,3,5-tricarboxylateHCID 75881—
Reactant3-(3-Tert-butyl-2-hydroxy-5-methylphenyl)-1-propanolHCID 13980953—
SolventDimethylformamideHCID 6228—
Product1,3,5-Tris[3-(3-tert-butyl-2-hydroxy-5-methylphenyl)propoxycarbonyl]benzeneHCID 1398096653%

Reaction Steps

Into a 100 ml reactor equipped with a condenser, thermometer and nitrogen introducing thin tube were charged 1.54 g (6.00 mmol) of trimethyl 1,3,5-benzenetricarboxylate, 4.00 g (18.00 mmol) of 3-(3-tert-butyl-2-hydroxy-5-methylphenyl)-1-propanol and 20 ml of N,N-dimethylformamide. The pressure of the reaction system was reduced to 20 mmHg and 75 vol% (15 ml) of N,N-dimethylformamide was distilled away to dry the reactants, solvent and apparatus. The reaction system was cooled to room temperature, and the vacuum was broken by introducing dry nitrogen. 0.07 g (1.8 mmol) of sodium amide was immediately added to initiate the ester exchange reaction. The reaction system was heated at 50° to 60° C. under 20 mmHg for 2 to 3 hours, and then heated at 60° to 80° C. under 20 mmHg for 2 to 3 hours while distilling N,N-dimethylformamide. Thereafter, the reaction mixture was further heated at 100° to 120° C. under 5 mmHg for 2 to 3 hours. When the reaction was completed, the reaction product was neutralized with dilute hydrochloric acid and then chloroform was added. After liquid separation and dehydration with anhydrous sodium sulfate, the organic solvent was removed under reduced pressure. After separation by silica gel chromatography (solvent: chloroform), 2.60 g (3.16 mmol) of the desired product was obtained. The yield was 53%. The physical properties of the product are shown below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04694102
Source datasetuspto-grants-1987_09
ORD IDord-08e31d1a63354fb7a51cd371504504a2
Source noteuspto-grants-1987_09