HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Nitrobenzoic Acid → 4-nitro-N-[3-(triethoxysilyl)propyl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Nitrobenzoic Acid | HCID 6108 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (3-Aminopropyl)triethoxysilane | HCID 13521 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-nitro-N-[3-(triethoxysilyl)propyl]benzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04860573 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-a54380c831bd451aab609b4981e89518 |
| Source note | uspto-grants-1989_08 |