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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442600Generated: November 2, 2026

Triethylamine → HCID 58610090, compound

https://huagongshe.com/reaction/1442600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantTributylphosphineHCID 13831—
ReactantSodium AzideHCID 33557—
ReactantHCID 58610098HCID 58610098—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 58610090HCID 5861009062.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

2-[(1,1′-Biphenyl-4-ylcarbonyl)thio]benzoic acid (1.15 g, 3.4 mmol) was suspended in acetone (10 ml). While stirring under ice cooling, triethylamine (0.49 g, 4.8 mmol) and then ethyl chloroformate (0.52 g, 3.8 mmol) were dropwise added to the suspension. After stirring at the same temperature for an hour, an aqueous solution (10 ml) of sodium azide (0.34 g, 5.2 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 (100 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and then filtered. The toluene solution was cooled to about −10° C. and tributylphosphine (0.84 g, 4.2 mmol) 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 15 minutes. The reaction solution was concentrated under reduced pressure and recrystallized from ethyl acetate-ethanol to give the title compound (0.67 g, 61%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659267B2
Source datasetuspto-grants-2010_02
ORD IDord-d7df067519844c98b4730ed121ebf2f8
Source noteuspto-grants-2010_02