Reaktion #51099

Reaktionsgleichung

2,2,2-trichloroethylchloroformate

Tetrahydroisoquinoline

triethylamine

→

title compound ( D6 )

Ausbeute 99.9%

3,4-Dihydro-1H-isoquinoline-2-carboxylic Acid 2,2,2-Trichloro-ethyl Ester

Ausbeute 99.9%

Lösungsmittel

dichloromethane

dichloromethane

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThe mixture was cooled in an ice bath
2. 2
   workup.ADDITIONAfter addition
3. 3
   WaschenThe solution was washed with 1M aqueous hydrochloric acid (2×100 ml)
4. 4
   Waschenwashed successively with water (100 ml), sodium bicarbonate (100 ml) and brine (50 ml)
5. 5
   Trocknendried (MgSO4)
6. 6
   Filtrationfiltered
7. 7
   Sonstigeevaporated

Vorschrift

Tetrahydroisoquinoline [Aldrich] (39.9 g, 300 mmol) was dissolved in dichloromethane (400 ml) and treated with triethylamine (32 g, 315 mmol). The mixture was cooled in an ice bath and a solution of 2,2,2-trichloroethylchloroformate (65.0 g, 306 mmol) in dichloromethane (100 ml) introduced dropwise over 15 minutes. After addition, the mixture was allowed to warm to room temperature and stirred for a further 30 minutes. The solution was washed with 1M aqueous hydrochloric acid (2×100 ml), then washed successively with water (100 ml), sodium bicarbonate (100 ml) and brine (50 ml), then dried (MgSO4), filtered and evaporated to give the title compound (D6) as a pale orange oil 92.5 g; δH (CDCl3 rotomers observed) ppm 2.90 (2H, app.t), 3.74-3.81 (2H, m), 4.67, 4.72 (2H, 2s), 4.80 (2H, s), 7.12-7.21 (4H, m).

Quelle