HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371275Generated: October 31, 2026
Succinic anhydride → HCID 67487353, compound
https://huagongshe.com/reaction/2371275
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 67486162 | HCID 67486162 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67487353 | HCID 67487353 | 5% |
Reaction Steps
To 3-(4-Amino-phenyl)-N-(4-benzofuran-2-yl-phenyl)-2-(4-tert-butyl-phenyl)-propionamide (100 mg, 0.2 mmol) in 2 ml diethyl ether, 2 ml toluene and 1 ml 1,4-dioxane was added succinic anhydride (22 mg, 0.22 mmol). The reaction mixture was stirred at 23° C. for 16 h, concentrated, and loaded to reverse phase silica gel. After chromatography (from 20% acetonitrile to 80% acetonitrile in water in 12 column volume), the fractions containing the desired product were collected and concentrated. The residue was diluted with methanol (1 ml) and water was added dropwise until the precipitate stop forming. The white precipitate was removed by filtration and dried under high vacuum at 50° C. to afford the title compound (6.3 mg, 5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08710236B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-6bdc15c309ef450aa250e4336b49356c |
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| Source note | uspto-grants-2014_04 |
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