HCID 10445534, compound → (2Z,6E)-3,7,11-Trimethyldodeca-2,6,10-trien-1-ol
Reaction equation
[CH3:1]/[C:2](/[CH2:9][CH2:10]/[CH:11]=[C:12](\[CH3:19])/[CH2:13][CH2:14][CH:15]=[C:16]([CH3:18])[CH3:17])=[CH:3]/[C:4](OCC)=[O:5].[H-].C([Al+]CC(C)C)C(C)C>C1(C)C=CC=CC=1>[CH3:1]/[C:2](/[CH2:9][CH2:10]/[CH:11]=[C:12](\[CH3:19])/[CH2:13][CH2:14][CH:15]=[C:16]([CH3:18])[CH3:17])=[CH:3]/[CH2:4][OH:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1 g (0.0038 mol) of ethyl (2Z,6E)-3,7,11-trimethyl-2,6,10-dodecatrienoate in 8 ml of toluene is treated dropwise at -5° to -10° with 9.45 ml of a solution of diisobutylaluminium hydride in toluene (1.2 mol/l). The solution is stirred at the same temperature for 1 hour under argon. The reaction mixture is poured into an ice-water mixture and extracted with ether. After drying and removing the solvent the residue is chromatographed on silica gel with ether-hexane 1:1. There is obtained (2Z,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-ol which has the following bands in the IR spectrum; 3326 cm-1, 1669 cm-1, 1446 cm-1, 1378 cm-1, 1000 cm-1.
Workup
- extractionextracted with ether
- customAfter drying
- customremoving the solvent the residue
- customis chromatographed on silica gel with ether-hexane 1:1
Sources & evidence
- ORD record
- ord-307ac752fe854034b77b2fffadbf6034
- Source dataset
- uspto-grants-1989_05
- Patent number
- US04827004
Reaction notes
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