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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187975Generated: November 1, 2026

Sodium Thiosulfate → HCID 67165552, compound

https://huagongshe.com/reaction/1187975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 67163960HCID 67163960—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67165552HCID 6716555236.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a solution of 0.24 g of methyl N-[4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-2-methylbenzoyl]carbamate synthesized in Synthetic Example 19 and 0.12 g of N-iodosuccinimide in 3 mL of N,N-dimethylformamide, 0.0112 g of palladium (II) acetate was added, and stirred under nitrogen atmosphere at 100° C. for 4 hours. After the completion of the reaction, the reaction mixture was poured in a solution of 0.03 g of sodium thiosulfate in 30 mL of water, and extracted with ethyl acetate (30 mL×1), the organic phase was dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that was eluated with ethyl acetate-hexane (gradient of 0:1 to 3:2) to obtain 0.11 g of the aimed product as colorless resinous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673951B2
Source datasetuspto-grants-2014_03
ORD IDord-349bc4b18d8d4c00bc04121cb7527b05
Source noteuspto-grants-2014_03