Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Xanthane hydride | HCID 2735329 | — |
| Reactant | HCID 14648350 | HCID 14648350 | — |
| Reactant | Ammonium chloride monohydrate | HCID 57429219 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59680527 | HCID 59680527 | 33% |
Reaction Steps
2-[3,4-Bis(octyloxy)phenyl]acetic acid (1.00 g, 2.55 mmol) was dissolved in tetrahydrofuran (8 ml), and 1,1′-carbonyidiimidazole (0.496 g, 3.06 mmol) was added thereto. The imidazole mixture was stirred for 1 hour at room temperature. Sodium hydride (60% oil suspension 0.102 g, 2.55 mmol) was suspended in tetrahydrofuran (8 ml), and 3-amino-1,2,4-dithiazole-5-thione (0.383 g, 2.55 mmol) was added thereto. After being stirred for 30 minutes at 0° C., the reaction mixture, with the imidazole mixture added thereto, was stirred for 16 hours at room temperature. The reaction mixture, with saturated ammonium chloride water added thereto, was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate water and saturated brine successively, dried over MgSO4, and then concentrated. The obtained residue was purified by silica gel column chromatography (chloroform), to give 2-[3,4-bis(octyloxy)phenyl]-N-(3-thioxo-3H-1,2,4-dithiazol-5-yl)acetoamide (Compound 10) (0.365 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07348017B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-5a5e5ff0a0d14c11aa045a8bb4dbdc1d |
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| Source note | uspto-grants-2008_03 |
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