Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723304Generated: November 2, 2026

4-Nitrobenzoic Acid → 4-nitro-N-[3-(triethoxysilyl)propyl]benzamide

https://huagongshe.com/reaction/1723304

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzoic AcidHCID 6108—
ReactantTriethylamineHCID 8471—
Reactant(3-Aminopropyl)triethoxysilaneHCID 13521—
ReactantThionyl ChlorideHCID 24386—
SolventDiethyl EtherHCID 3283—
Product4-nitro-N-[3-(triethoxysilyl)propyl]benzamideHCID 109028—

Reaction Steps

p-nitrobenzoic acid (10 g; 60 mmol) was added to 15 g thionylchloride. This mixture was heated during 2 h under reflux. Subsequently the thionylchloride was removed at reduced pressure. To the remainder γ-aminopropyltriethoxysilane (13,3 g; 60 mmol) was added, dissolved in 50 ml diethylether with 10 g triethylamine. After 2 h agitation at room temperature, the mixture was filtered. The filtrate was evaporated at reduced pressure. The remainder was washed in water, filtered, and dried at reduced pressure over KOH. Yield: 9,5 g (43%). Melting point 99° . . . 105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04860573
Source datasetuspto-grants-1989_08
ORD IDord-a54380c831bd451aab609b4981e89518
Source noteuspto-grants-1989_08