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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442584Generated: November 1, 2026

Triethylamine → HCID 58610102, compound

https://huagongshe.com/reaction/1442584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantTributylphosphineHCID 13831—
ReactantSodium AzideHCID 33557—
ReactantHCID 58610111HCID 58610111—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 58610102HCID 5861010240.2%

Reaction Conditions

Temperature-15 °C

Reaction Steps

2-[(Cyclobutylcarbonyl)thio]benzoic acid (9.01 g, 38 mmol) was suspended in acetone (150 ml). While stirring under ice cooling, triethylamine (4.25 g, 42 mmol) and then ethyl chloroformate (4.88 g, 45 mmol) were dropwise added to the suspension. After stirring at the same temperature for an hour, an aqueous solution (15 ml) of sodium azide (2.92 g, 45 mmol) was dropwise added to the reaction mixture, followed by further stirring for an hour. The reaction mixture was diluted with water and the dilution was extracted with toluene. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and then filtered. The toluene solution was cooled to about −15° C. and a solution (15 ml) of tributylphosphine (7.70 g, 38 mmol) in toluene was dropwise added to the solution. After completion of the dropwise addition, the reaction temperature was reverted to room temperature and the mixture was heated under reflux for 10 minutes. The reaction solution was concentrated under reduced pressure. The residue was recrystallized from toluene-isopropyl ether to give the title compound (3.32 g, 40%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659267B2
Source datasetuspto-grants-2010_02
ORD IDord-0db0e3c709354c2ab18c009147bcfb5a
Source noteuspto-grants-2010_02