HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245383Generated: October 31, 2026
3,3-Dimethylbutanoyl chloride → HCID 178429851, compound
https://huagongshe.com/reaction/2245383
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,3-Dimethylbutanoyl chloride | HCID 81514 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-Methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imine | HCID 86619167 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178429851 | HCID 178429851 | — |
Reaction Steps
To a solution of 5-methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imine (Example 22C, 0.14 g, 0.44 mmol) in acetonitrile (3 mL) was added Hunig's base (0.062 g, 0.48 mmol) followed by 3,3-dimethylbutanoyl chloride (0.088 g, 0.66 mmol). The mixture was heated for 12 hours at 65° C. The reaction mixture was cooled down, diluted with CH2Cl2 (50 mL), and washed with water and brine. The organic phase was dried over sodium sulfate, filtered and dried. After evaporation under reduced pressure, the residue was chromatographed over silica using CH2Cl2-5%MeOH/CH2Cl2 to supply the titled compound. 1H NMR (CDCl3) δ ppm 1.00 (9H), 2.35 (2H), 4.65 (2H), 5.25 (1H), 5.35 (1H), 7.15 (1H), 7.25 (1H), 7.55 (1H); MS (ESI) m/z 419 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683084B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-e84f01c3145b41cfb2d4c7a1235316c3 |
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| Source note | uspto-grants-2010_03 |
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