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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1187979Generated: October 31, 2026

Methyl chloroformate → HCID 24895908, compound

https://huagongshe.com/reaction/1187979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
ReactantHCID 67163725HCID 67163725—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24895908HCID 2489590851.8%

Reaction Steps

In a solution of 0.50 g of N-[4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-methyl benzoyl]-N′-ethyl urea synthesized similarly to Synthetic Example 26 in 4 mL of tetrahydrofuran, 4 mL of 1M tetrahydrofuran solution of lithium hexamethyl disilazane was added at −78° C. with stirring, and stirred at the same temperature for 30 minutes. Then, 0.12 g of methyl chloroformate was added in the reaction mixture at −78° C. with stirring. After the completion of the addition dropwise, it was continued to stir further for 18 hours while the temperature was slowly raised to room temperature. After the completion of the reaction, 30 mL of ice water was added, and extracted with ethyl acetate (30 mL×2). The organic phase was dehydrated with and dried over saturated sodium chloride aqueous solution and 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 1:2) to obtain 0.29 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-e17cb49d2a884d879d7bbc72b4ae62b3
Source noteuspto-grants-2014_03