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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923528Generated: October 31, 2026

4-(Heptyloxy)benzoyl chloride → 4-((4-Nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoate

https://huagongshe.com/reaction/923528

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Heptyloxy)benzoyl chlorideHCID 2724182—
ReactantN-(4-hydroxybenzyl)-4-nitrobenzamideHCID 12714523—
SolventDichloromethaneHCID 6344—
Product4-((4-Nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoateHCID 8925304173%

Reaction Steps

Prepared using General Procedure 2: To a stirring solution of N-(4-hydroxybenzyl)-4-nitrobenzamide INT-1 (647 mg, 2.38 mmol) in DCM (10 mL) at 0° C. was added TEA (1.03 mL, 7.13 mmol) followed by 4-(heptyloxy)benzoyl chloride (12.4 mL, 2.85 mmol). The suspension was sonicated until clear then diluted with DCM (50 mL) and washed with NaHCO3 (20 mL). The organic layer was concentrated and purified by chromatography (EA/hexanes) to provide 857 mg (73%) of 4-((4-nitrobenzamido)methyl)phenyl 4-(heptyloxy)benzoate INT-2. LCMS-ESI (m/z) calculated for C28H30N2O6: 490; found 491 [M+H]+, tR=3.41 min (Method 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278910B2
Source datasetuspto-grants-2016_03
ORD IDord-d14024c373c8414da7ec56315486a940
Source noteuspto-grants-2016_03