Water → 13-Ethyl-17beta-(2-hydroxyethoxy)-3-methoxygona-2,5(10)-diene

HRID 1415029Notes

Reaction equation

HRID 1415029 reaction equation
[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C:12]4[CH:13]=[CH:14][C:15]([O:20][CH3:21])=[CH:16][C:17]=4[CH2:18][CH2:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][C@@H:4]2[O:22][CH2:23][CH2:24][OH:25])[CH3:2].[Li].[Cl-].[NH4+].O>COCC(O)C.O1CCCC1.N>[CH2:1]([C@:3]12[CH2:11][CH2:10][C@@H:9]3[C:12]4[CH2:13][CH:14]=[C:15]([O:20][CH3:21])[CH2:16][C:17]=4[CH2:18][CH2:19][C@H:8]3[C@@H:7]1[CH2:6][CH2:5][C@@H:4]2[O:22][CH2:23][CH2:24][OH:25])[CH3:2]

Participants

8

Procedure

Dissolve dl-13-ethyl-17β-(2-hydroxyethoxy)-3-methoxygona-1,3,5(10)-triene (4.0 g) in 1-methoxy-2-propanol (60 ml), tetrahydrofuran (120 ml) and liquid ammonia (300 ml). Gradually add lithium (4.0 g) with stirring over a period of 1 hour. Add ammonium chloride (8.0 g) and water. Filter, wash and dry the resulting precipitate. Dissolve the product in tetrahydrofuran (300 ml) and liquid ammonia (300 ml) and treat with lithium (4.0 g). Stir for 1 hour. Add absolute ethanol, then water. Filter the resulting precipitate and wash it with water to obtain dl-13-ethyl-17β-(2-hydroxyethoxy)-3-methoxygona-2,5(10)-diene (3.4 g); essentially no ultraviolet absorption at the 280 mμ region, infrared absorption maxima at 2.91 μ, 5.89 μ, 6.0 μ.

Workup

  1. filtrationFilter
  2. washwash
  3. customdry the resulting precipitate
  4. dissolutionDissolve the product in tetrahydrofuran (300 ml)
  5. additionliquid ammonia (300 ml) and treat with lithium (4.0 g)
  6. additionAdd absolute ethanol
  7. filtrationFilter the resulting precipitate
  8. washwash it with water

Sources & evidence

ORD record
ord-293d70b8162c4d12b2855e66d7d789bd
Source dataset
uspto-grants-1977_01
Patent number
US04002746

Reaction notes

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