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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247664Generated: October 30, 2026

4-Isobutylbenzoic acid → HCID 68525595, compound

https://huagongshe.com/reaction/2247664

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Isobutylbenzoic acidHCID 38111—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-{[t-Butyl(dimethyl)silyl]oxy}-N'-hydroxy-4,5,6,7-tetrahydro-1-benzofuran-2-carboximidamideHCID 86620215—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68525595HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-ba1ec5db613a4e40a3ff416842aaf89b
Source noteuspto-grants-2010_03