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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257993Generated: October 25, 2026

Triethylamine → HCID 87233421, compound

https://huagongshe.com/reaction/1257993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chlorothioformateHCID 18056—
ReactantHCID 178428868HCID 178428868—
SolventTetrahydrofuranHCID 8028—
ProductHCID 87233421HCID 8723342166%

Reaction Steps

To a solution of 5-hydroxy-1-methylpyrazol-4-yl 3-(4,5-dihydroisoxazol-3-yl)-2-methyl-4-(methylsulfonyl)phenyl ketone (100 mg, 2.75×10−4 mol) in anhydrous tetrahydrofuran (5 mL) were added triethylamine (55 mg) and 96% S-ethyl chlorothiolformate (45 mg) at room temperature. After the reaction solution was stirred for 1 hour, 150 mL of ethyl acetate was added, and the solution was washed twice with a saturated brine. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=6:4) to obtain the desired product (82 mg) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466088B2
Source datasetuspto-grants-2013_06
ORD IDord-93c863f9e06e477fb60470aac27052b9
Source noteuspto-grants-2013_06