Triethylamine → HCID 4462779, compound

Temperature

-10 °C

2-{[2-(Methoxy)benzoyl]thio}benzoic acid (1.90 g, 3.5 mmol) was suspended in acetone (10 ml). While stirring under ice cooling, triethylamine (0.93 g, 9.2 mmol) and then ethyl chloroformate (0.99 g, 7.3 mmol) were dropwise added to the suspension. After stirring at the same temperature for an hour, an aqueous solution (10 ml) of sodium azide (0.64 g, 9.9 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 (1.60 g, 7.9 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 ethanol to give the title compound (0.99 g, 56%) as crystals.

1. stirringAfter stirring at the same temperature for an hour
2. stirringby further stirring for an hour
3. extractionthe dilution was extracted with toluene (100 ml×2)
4. washThe extract was washed with saturated brine
5. dry with materialdried over anhydrous magnesium sulfate
6. filtrationfiltered
7. additionAfter completion of the dropwise addition
8. customwas reverted to room temperature
9. temperaturethe mixture was heated
10. temperatureunder reflux for 15 minutes
11. concentrationThe reaction solution was concentrated under reduced pressure
12. customrecrystallized from ethanol

ORD record

ord-a8cac683d527444bb44246d2999d4014

Source dataset

uspto-grants-2010_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07659267B2