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In the asymmetric unit of the title compound, C38H56O3, there are two symmetry-independent mol­ecules that differ in the rotation angle along the C—O bond between the 3-(4-eth­oxy­phen­yl)prop-2-enoate and cholest-5-en-3β-yl groups by 169.3 (3)°. In both mol­ecules, steroid ring B adopts a half-chair conformation, rings A and C adopt a chair conformation and ring D exists in an envelope form. The two symmetry-independent mol­ecules pack in the crystal into separate layers parallel to (-102) with their long axis parallel to the [201] direction. Short inter­molecular C—H...O and C—H...π contacts are observed.

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In the title mol­ecule, C10H11NO2, the benzene ring forms dihedral angles of 33.15 (2) and 6.20 (2)° with the mean planes of the amide and propen­oxy groups, respectively. The amide –NH2 group is oriented toward the propen­oxy substituent and forms a weak intra­molecular N—H...O hydrogen bond to the propen­oxy O atom. The conformation of the propen­oxy group at the Csp2—Csp3 and Csp3—O bonds is synperiplanar and anti­periplanar, respectively. In the crystal, N—H...O hydrogen bonds involving the amide groups generate C(4) and R23(7) motifs that organize the mol­ecules into tapes along the a-axis direction. There are C—H...π inter­actions between the propen­oxy –CH2 group and the aromatic system of neighboring mol­ecules within the tape. The mean planes of the aromatic ring and the propen­oxy group belonging to mol­ecules located on opposite sites of the tape form an angle of 83.16 (2)°.
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