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ChemicalBook CAS DataBase List N-CAPRIC ACID N-DECYL ESTER
1654-86-0

N-CAPRIC ACID N-DECYL ESTER synthesis

13synthesis methods
Method 1: n-decanoic acid n-decyl ester was prepared as follows: 1 mol n-decanol and 1 mol n-decanoic acid and 0.22 g 0.22 g 2001 (tin oxalate) were heated in an aqueous separator at a temperature of 240 °C for 3 hours. The product was evaporated via a 30
-

Yield:1654-86-0 99%

Reaction Conditions:

with sodium bromate;sulfuric acid;sodium bromide in water at 20; for 24 h;

Steps:

General procedure for octyl octanoate (2a)

General procedure: A total of 1.0 g of 1-octanol (7.69 mmol) was taken in a 50-mL round-bottomed flask, to it NaBr 0.523 g (0.66 eq.), NaBrO 3 0.383 g (0.33 eq.), and 10 mL of H 2 O [comprises the bromide and bromate in 2:1 molar ratio] were added[6f]. The reaction mixture was stirred vigorously to dissolve the contents completely. To the above reaction mixture, the aqueous H 2 SO 4 solution (0.5 eq.) was added slowly under stirring over a period of 2.5 h at room temperature (prepared by adding 0.21 mL of 98% H 2 SO 4 to 1 mL of water). The reaction mixture was allowed to stir for up to 24 h. After the completion of reaction, the product was extracted with CH 2 Cl 2 (3 15 mL), the organic layer was dried with Na 2 SO 4 and removal of the solvent obtained octyloctanoate in 98% yield (0.953 g) as colorless liquid. The product was confirmed by GC-MS as well as by NMR.

References:

Reddy, N. Naresh Kumar;Ravi, Chitrakar;Adimurthy, Subbarayappa [Synthetic Communications,2018,vol. 48,# 13,p. 1663 - 1670]

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