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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260363Generated: November 3, 2026

3,3-Dimethylbutanoyl chloride → HCID 178429851, compound

https://huagongshe.com/reaction/1260363

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Methylene-3-(2,2,3,3-tetrafluoro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)thiazolidin-2-imineHCID 86619167—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 178429851HCID 178429851—

Reaction Conditions

Temperature65 °C

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 (9 H), 2.35 (2 H), 4.65 (2 H), 5.25 (1 H), 5.35 (1 H), 7.15 (1 H), 7.25 (1 H), 7.55 (1 H); MS (ESI) m/z 419(M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470813B2
Source datasetuspto-grants-2013_06
ORD IDord-d8612ba2949945878f8513182fc6e3cc
Source noteuspto-grants-2013_06