Tributylstannane → Acetate

HRID 2229963Notes

Reaction equation

HRID 2229963 reaction equation
C([SnH](CCCC)CCCC)CCC.Br[CH:15]1[CH2:20][CH2:19][CH2:18][CH2:17][CH:16]1[OH:21].[C:22]([O:30][CH:31]1[CH2:36][C:35]([CH3:38])([CH3:37])[N:34]([OH:39])[C:33]([CH3:41])([CH3:40])[CH2:32]1)(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.CCCCCCC>ClC1C=CC=CC=1>[C:22]([O-:30])(=[O:29])[CH3:23].[C:22]([O:30][CH:31]1[CH2:32][C:33]([CH3:40])([CH3:41])[N:34]([O:39][CH:15]2[CH2:20][CH2:19][CH2:18][CH2:17][CH:16]2[OH:21])[C:35]([CH3:38])([CH3:37])[CH2:36]1)(=[O:29])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1

Participants

7

Procedure

Tributyltin hydride is added dropwise to a solution of 2-bromocyclohexanol and excess 4-benzoyloxy-1-oxyl-2,2,6,6-tetramethylpiperidine in chlorobenzene. The mixture is heated to facilitate reaction. The crude reaction mixture is passed through silica gel with heptane and then heptanelethyl acetate to afford the title compound as a mixture os cis/trans isomers.

Workup

  1. temperatureThe mixture is heated
  2. customreaction
  3. customThe crude reaction mixture

Sources & evidence

ORD record
ord-a9a903cb597144bcbdf2d3097cd59b30
Source dataset
uspto-grants-2002_07
Patent number
US06420463B1

Reaction notes

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