HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247664Generated: October 30, 2026
4-Isobutylbenzoic acid → HCID 68525595, compound
https://huagongshe.com/reaction/2247664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Isobutylbenzoic acid | HCID 38111 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 4-{[t-Butyl(dimethyl)silyl]oxy}-N'-hydroxy-4,5,6,7-tetrahydro-1-benzofuran-2-carboximidamide | HCID 86620215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68525595 | HCID 68525595 | — |
Reaction Steps
The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 5 (5a) using 4-isobutylbenzoic acid (0.12 g, 0.66 mmol), 1-hydroxybenzotriazole (0.11 g, 0.78 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.14 g, 0.72 mmol), 4-{[t-butyl(dimethyl)silyl]oxy}-N′-hydroxy-4,5,6,7-tetrahydro-1-benzofuran-2-carboximidamide (0.19 g, 0.6 mmol) that was obtained in Example 7 (7d), and tetrabutylammonium fluoride (a 1.0 M solution in tetrahydrofuran, 1.2 ml, 1.2 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:2-1:1) as the eluent to afford the title compound (0.15 g) in a yield of 75% as a pale yellowish oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07687491B2 |
|---|
| Source dataset | uspto-grants-2010_03 |
|---|
| ORD ID | ord-ba1ec5db613a4e40a3ff416842aaf89b |
|---|
| Source note | uspto-grants-2010_03 |
|---|