Réaction #927253

Équation de réaction

1-(7-carboxyheptyl)-cyclopropene

Triethylamine

methylchloroformate

→

7-cycloprop-1-enyl-heptanoic acid ethyl ester

Rendement 75.0%

Solvants

ether

Conditions de réaction

Traitement

1. 1
   Autrethe reaction mixture was transferred to a separatory funnel
2. 2
   LavageThe ether phase was washed with water (2×) and brine
3. 3
   Séchagedried over magnesium sulfate
4. 4
   Filtrationfiltered
5. 5
   workup.DISSOLUTIONThe product was dissolved in ethanol
6. 6
   Températurecooled in an ice bath
7. 7
   workup.ADDITIONtreated with 1 ml of a 21% sodium ethoxide in ethanol solution
8. 8
   workup.ADDITIONwater and ether were added
9. 9
   LavageThe ether phase was washed with 1N sodium hydroxide solution, water, and brine
10. 10
    Séchagedried over magnesium sulfate
11. 11
    Filtrationfiltered

Mode opératoire

A solution of 220 mg (1.3 mmol) of 1-(7-carboxyheptyl)-cyclopropene in ether was cooled to 0° C. Triethylamine (0.20 g, 2 mmol) was added, then 0.12 g (1.3 mmol) of methylchloroformate was added. After 2 hours at 0° C., the reaction mixture was transferred to a separatory funnel. The ether phase was washed with water (2×) and brine, dried over magnesium sulfate, filtered and stripped. The product was dissolved in ethanol, cooled in an ice bath and treated with 1 ml of a 21% sodium ethoxide in ethanol solution. The reaction mixture was stirred ½ hour, then water and ether were added. The ether phase was washed with 1N sodium hydroxide solution, water, and brine, dried over magnesium sulfate, filtered and stripped to give 10 mg of 75% pure 7-cycloprop-1-enyl-heptanoic acid ethyl ester.

Source