HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187987Generated: November 1, 2026
Dimethylformamide dimethyl acetal → HCID 152771638, compound
https://huagongshe.com/reaction/1187987
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | HCID 67164677 | HCID 67164677 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 152771638 | HCID 152771638 | 69% |
Reaction Steps
In a solution of 0.09 g of 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methoxymethyl benzoic acid amide in 2 mL of tetrahydrofuran, 0.05 g of N,N-dimethylformamide dimethylacetal was added, and stirred at room temperature for 2 hours. After the completion of the reaction, the solvent was distilled off under reduced pressure, and the residue was dissolved in 2 mL of tetrahydrofuran, a solution of 0.02 g of methoxyamine hydrochloride in 2 mL of water was added dropwise. After the completion of the addition dropwise, it was continued to stir at room temperature further for 30 minutes. After the completion of the reaction, the solvent was distilled off under reduced pressure, 5 mL of water was added in the residue, and extracted with ethyl acetate (10 mL×1). The organic phase was dehydrated with and dried over saturated sodium chloride aqueous solution and then anhydrous sulfuric acid, and the solvent was distilled off under reduced pressure. The residue was purified with silica gel column chromatography that were eluated with ethyl acetate-hexane (1:4) to obtain 0.07 g of the aimed product as white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08673951B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-8ec67870d2ce4284a8e406c270fdbe07 |
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| Source note | uspto-grants-2014_03 |
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