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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442587Generated: November 1, 2026

Triethylamine → HCID 58610103, compound

https://huagongshe.com/reaction/1442587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantTributylphosphineHCID 13831—
ReactantSodium AzideHCID 33557—
ReactantHCID 86603552HCID 86603552—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 58610103HCID 5861010330%

Reaction Conditions

Temperature-15 °C

Reaction Steps

2-[(Isopropylcarbonyl)thio]benzoic acid (11.20 g, 50 mmol) was suspended in acetone (150 ml). While stirring under ice cooling, triethylamine (5.10 g, 50 mmol) and then ethyl chloroformate (6.68 g, 62 mmol) were dropwise added to the suspension. After stirring at the same temperature for an hour, an aqueous solution (15 ml) of sodium azide (5.00 g, 77 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×3). 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 (10 ml) of tributylphosphine (10.50 g, 52 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 15 minutes. The reaction solution was concentrated under reduced pressure. The residue was recrystallized from ethanol-ethyl acetate to give the title compound (3.03 g, 30%) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659267B2
Source datasetuspto-grants-2010_02
ORD IDord-764617329e3b46fc98a5dd8c62b85d49
Source noteuspto-grants-2010_02