HCID 11558022, compound → (2E,6Z)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol

HRID 1761755Notes

Reaction equation

HRID 1761755 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

Procedure

A solution of 1 g (0.0038 mol) of ethyl (2E,6Z)-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, i.e. 3.0 mol equivalents). 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 (2E,6Z)-3,7,11-trimethyl-2,6,10-dodecatrien-1-ol which has the following bands in the IR spectrum: 3323 cm-1, 1668 cm-1, 1446 cm-1, 1377 cm-1, 1001 cm-1.

Workup

  1. extractionextracted with ether
  2. customAfter drying
  3. customremoving the solvent the residue
  4. customis chromatographed on silica gel with ether-hexane 1:1

Sources & evidence

ORD record
ord-c6cfa93cd4e1456a812547a0f72710ff
Source dataset
uspto-grants-1989_05
Patent number
US04827004

Reaction notes

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