Methane → HCID 22854044, compound
Reaction equation
[OH:1][C:2]1([C:27]#[C:28][C:29]([OH:31])=[O:30])[CH2:7][CH2:6][C@:5]2([OH:26])[C@H:8]3[C@H:18]([CH2:19][CH2:20][C@:3]12[CH3:4])[C@:16]1([CH3:17])[C@@H:11]([CH2:12][C@@H:13]([O:21][CH2:22][O:23][CH2:24][CH3:25])[CH2:14][CH2:15]1)[CH2:10][CH2:9]3.C>C(O)C.[Pd]>[OH:1][C:2]1([CH2:27][CH2:28][C:29]([OH:31])=[O:30])[CH2:7][CH2:6][C@:5]2([OH:26])[C@H:8]3[C@H:18]([CH2:19][CH2:20][C@:3]12[CH3:4])[C@:16]1([CH3:17])[C@@H:11]([CH2:12][C@@H:13]([O:21][CH2:22][O:23][CH2:24][CH3:25])[CH2:14][CH2:15]1)[CH2:10][CH2:9]3Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 17-hydroxy-17-carboxyethynyl-3beta-ethoxymethoxy-14-hydroxy-5beta,14beta-androstane (30 mg), prepared as described in Example 12, in ethanol (5 ml), was hydrogenated at 2.72 atmosphere in a Parr apparatus in the presence of 10% palladium over charcoal.
Sources & evidence
- ORD record
- ord-dedaec85bf7843bc866a0ca2b2d1f275
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05426179
Reaction notes
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