HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067626Generated: November 2, 2026
Dimethylformamide dimethyl acetal → HCID 58031425, compound
https://huagongshe.com/reaction/2067626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 58031569 | HCID 58031569 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58031425 | HCID 58031425 | 98% |
Reaction Steps
To a solution of 1-(5-acetyl-4-methylthiazol-2-yl)-3-(4-(trifluoromethyl)benzyl)-imidazolidin-2-one (1.00 g, 2.60 mmol) in N,N-dimethylformamide (20 mL) was added N,N-dimethylformamide dimethyl acetal (0.45 mL, 3.17 mmol). The reaction mixture was heated at 110° C. for 18 hours. The solvent was removed in vacuo, and the residue was washed with water to afford the title compound in 98% yield (1.12 g): 1H NMR (300 MHz, DMSO-d6) δ 7.70 (d, J=8.1 Hz, 2H), 7.60 (d, J=8.1 Hz, 2H), 7.58 (d, J=12.0 Hz, 1H), 5.28 (d, J=12.0 Hz, 1H), 4.50 (s, 2H), 4.01-3.95 (m, 2H), 3.48-3.43 (m, 2H), 3.08 (s, 3H), 2.81 (s, 3H), 2.48 (s, 3H); MS (ES+) m/z 439.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293768B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-68660dcca092497eb5785d1f0cd9fc73 |
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| Source note | uspto-grants-2012_10 |
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