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ChemicalBook CAS DataBase List Nandrolone phenylpropionate
62-90-8

Nandrolone phenylpropionate synthesis

5synthesis methods
Nandrolone phenylpropionate is prepared by reacting anhydrous MeCN with a mixture of 3-phenylpropanoic acid, aryneprecursor, nandrolone CsF, K2CO3, and 18-crown-6 in 70 ℃ in an oil bath.
Add anhydrous MeCN (0.5 mL) to a mixture of 3-phenylpropanoic acid (30.0 mg, 0.2 mmol, 1.0 equiv), aryneprecursor (119.2 mg, 0.4 mmol, 2.0 equiv), nandrolone (82.3 mg, 0.3 mmol, 1.5 equiv), CsF (182.3 mg, 1.2 mmol, 6.0 equiv), K2CO3 (82.9 mg, 0.6 mmol, 3.0 equiv), and 18-crown-6 (158.6 mg, 0.6 mmol, 3.0 equiv). Warm the mixture to 70 ℃ in an oil bath and stir at this temperature for8 hours. Remove all the volatiles directly on rotary evaporator. Purify by flash column chromatography with pet ether:EtOAc = 20:1. 1H NMR (400 MHz, CDCl3) δ 7.31-7.26(m,2H), 7.23-7.17(m,3H), 5.83 (s, lH), 4.65-4.58(m, lH), 2.95(t, J= 8.0 Hz,2H), 2.64(t, J= 8.0 Hz,2H), 2.51-2.36(m, 2H), 2.31-2.04(m, 5H), 1.86-1.79(m, 2H), 1.72-1.61 (m, 2H), 1.57-1.00(m, 8H),0.90-0.81(m, 1H), 0.79 (s, 3H)ppm.
Fig The synthetic method 1 of Nandrolone phenylpropionate
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Yield:62-90-8 74%

Reaction Conditions:

with bis(1-butyl-3-methylimidazolium) tungstate in 1,4-dioxane at 120; for 2.5 h;

Steps:

6

In a 100 ml reaction flask, 0.397 g (3 mmol) of cinnamaldehyde, 0.411 g (1.5 mmol) of Nandrolone, 0.158 g (0.3 mmol) of [Bmim] 2 [WO4] catalyst, and 10 ml of 1,4-dioxane were added and heated. After heating to 120 ° C, the reaction was carried out for 2.5 h. After the reaction was completed, it was cooled to room temperature, extracted with 30 ml of water and 20 ml of ethyl acetate, and the phases were allowed to stand, and the organic phase was concentrated to obtain the target. The product, a yield of 74%.

References:

CN109678718,2019,A Location in patent:Paragraph 0035

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