HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247738Generated: November 2, 2026
4-Phenoxybenzoic acid → HCID 68521959, compound
https://huagongshe.com/reaction/2247738
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenoxybenzoic acid | HCID 75182 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 86620224 | HCID 86620224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68521959 | HCID 68521959 | — |
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-phenoxybenzoic acid (0.16 g, 0.73 mmol), 1-hydroxybenzotriazole (0.12 g, 0.76 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.15 g, 0.76 mmol), 4-ethyl-N′-hydroxy-5-[(tetrahydro-2H-pyran-2-yloxy)methyl]thiophene-2-carboximidamide (0.17 g, 0.69 mmol) that was obtained in Example 22 (22d) and tetrabutylammonium fluoride (a 1.0 M solution in tetrahydrofuran, 14 ml, 1.4 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 (0:10 to 2:8) as the eluent to afford the title compound (0.25 g) in a yield of 78% as a colourless oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687491B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-2ce976adf07b40d1879e56f89a27df2b |
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| Source note | uspto-grants-2010_03 |
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