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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389144Generated: October 31, 2026

Bromotrichloromethane → HCID 58243993, compound

https://huagongshe.com/reaction/389144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrichloromethaneHCID 6383—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(Bis(2-methoxyethyl)amino)sulfur trifluorideHCID 2734690—
ReactantHCID 58243700HCID 58243700—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 58243993HCID 5824399377.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Methyl N-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)benzoyl]-L-serinate (1.41 g) was mixed with dichloromethane (45 ml), followed by cooling to −78° C. under a nitrogen atmosphere. 2-methoxy-N-(2-methoxyethyl)-N-(trifluoro-λ4-sulfanyl)ethanamine (0.580 ml) was added thereto, followed by stirring for 2 hours, and bromo(trichloro)methane (0.920 ml) and DBU (1.40 ml) were sequentially added thereto at 0° C., followed by stirring for 3 hours. The reaction solution was diluted with ethyl acetate, washed with water, saturated aqueous sodium bicarbonate solution and then saturated brine in this order, and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=100:1). The resulting solid was washed with diisopropylether to obtain, as a white solid, methyl 2-[5-chloro-2-(1-methyl-1-{4-methyl-5-[2-(trifluoromethyl)phenyl]-4H-1,2,4-triazol-3-yl}ethoxy)phenyl]-1,3-oxazole-4-carboxylate (1.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377923B2
Source datasetuspto-grants-2013_02
ORD IDord-1a0086e4fe97477bae9d32e731452c28
Source noteuspto-grants-2013_02