Iodine → HCID 53924134, compound
Reaction equation
[OH:1][C@@H:2]1[CH2:21][CH2:20][C@@:19]2([CH3:22])[C@@H:4]([CH2:5][CH2:6][C@@H:7]3[C@@H:18]2[CH2:17][CH2:16][C@@:15]2([CH3:23])[C@H:8]3[CH2:9][C@@H:10]([CH3:24])[C@@H:11]2[C:12](=[O:14])[CH3:13])[CH2:3]1.C(Cl)(Cl)(Cl)Cl.[O-2].[Ca+2].[I:32]I>CO.[Cl-].[Ca+2].[Cl-].C1COCC1>[OH:1][C@@H:2]1[CH2:21][CH2:20][C@@:19]2([CH3:22])[C@@H:4]([CH2:5][CH2:6][C@@H:7]3[C@@H:18]2[CH2:17][CH2:16][C@@:15]2([CH3:23])[C@H:8]3[CH2:9][C@@H:10]([CH3:24])[C@@H:11]2[C:12](=[O:14])[CH2:13][I:32])[CH2:3]1Participants
8
Procedure
A mixture of 3α-hydroxy-16α-methyl-5α-pregnan-20-one (21 g) methanol (80 ml), carbon tetrachloride (40 ml), THF (120 ml), calcium oxide (25 g) and calcium chloride in methanol (10%, 3 ml) is stirred at 25°-30°. A solution of iodine (20 g) in calcium chloride (10%, 70 ml) is added to the steroid mixture over 1 hr. The mixture is stirred an additional 2 hr at 30°, filtered through a pad of filter aid, and the filtrate concentrated under reduced pressure to an oil. The oil is dissolved in methylene chloride and flash chromatographed over silica gel (100 g) eluting with methylene chloride/ethyl acetate (4/1). The appropriate fractions are pooled, concentrated and the residue triturated with ether to give the title compound.
Workup
- stirringThe mixture is stirred an additional 2 hr at 30°
- filtrationfiltered through a pad of filter aid
- concentrationthe filtrate concentrated under reduced pressure to an oil
- dissolutionThe oil is dissolved in methylene chloride
- customflash chromatographed over silica gel (100 g)
- washeluting with methylene chloride/ethyl acetate (4/1)
- concentrationconcentrated
- customthe residue triturated with ether
Sources & evidence
- ORD record
- ord-262f4c4471ab42cb8102de9f194b42b5
- Source dataset
- uspto-grants-1995_01
- Patent number
- US05380840
Reaction notes
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