Sodium Hydroxide → HCID 15871125, compound

HRID 1764971Notes

Reaction equation

HRID 1764971 reaction equation
[C-:1]#[N:2].C([Al+]CC)C.[CH3:8][CH:9]([CH2:11][CH2:12][CH2:13][C@H:14]([C@@H:16]1[C@:33]2([CH3:34])[C@H:19]([C:20]3[CH2:21][CH2:22][C:23]4[C@:28]([C:30]=3[CH2:31][CH2:32]2)([CH3:29])[CH2:27][CH2:26][C:25](=[O:35])[CH:24]=4)[CH2:18][CH2:17]1)[CH3:15])[CH3:10].[OH-].[Na+]>O1CCCC1>[C:1]([C@@:23]12[CH2:24][C:25](=[O:35])[CH2:26][CH2:27][C@:28]1([CH3:29])[C:30]1[CH2:31][CH2:32][C@@:33]3([CH3:34])[C@@H:19]([CH2:18][CH2:17][C@@H:16]3[C@H:14]([CH3:15])[CH2:13][CH2:12][CH2:11][CH:9]([CH3:8])[CH3:10])[C:20]=1[CH2:21][CH2:22]2)#[N:2].[C:1]([C@:23]12[CH2:24][C:25](=[O:35])[CH2:26][CH2:27][C@:28]1([CH3:29])[C:30]1[CH2:31][CH2:32][C@@:33]3([CH3:34])[C@@H:19]([CH2:18][CH2:17][C@@H:16]3[C@H:14]([CH3:15])[CH2:13][CH2:12][CH2:11][CH:9]([CH3:8])[CH3:10])[C:20]=1[CH2:21][CH2:22]2)#[N:2]

Participants

6

Procedure

30 ml of a diethylaluminum cyanide solution (1 N, in toluene) are added to a solution of 3.82 g cholesta-4,8-dien-3-one in 60 ml tetrahydrofuran at 0° C. The reaction mixture is warmed to room temperature and stirred for 4 hours. 20 ml of a sodium hydroxide solution (1 N) are added before the mixture is extracted with diethyl ether. The organic layer is separated, dried over anhydrous sodium sulphate and filtered. After evaporation of the solvent the residue is chromatographed with a mixture of hexane and ethyl acetate to give 1.46 g 5-cyano-5β-cholest-8-en-3-one and 1.76 g 5-cyano-5α-cholest-8-en-3-one as pale yellow crystals.

Workup

  1. extractionis extracted with diethyl ether
  2. customThe organic layer is separated
  3. dry with materialdried over anhydrous sodium sulphate
  4. filtrationfiltered
  5. customAfter evaporation of the solvent the residue
  6. customis chromatographed with a mixture of hexane and ethyl acetate

Sources & evidence

ORD record
ord-faf64b449a944200b02f52d7b2be471a
Source dataset
uspto-grants-2007_06
Patent number
USRE039678E1

Reaction notes

Loading…