Myrcene → (Z)-2,6-dimethyloct-2-ene-1,8-diol
Reaction equation
[CH3:1][C:2]([CH3:10])=[CH:3][CH2:4][CH2:5][C:6]([CH:8]=[CH2:9])=[CH2:7].ClC(CCCCC)C(Cl)=C(C)C.C([O-])(=O)C.[Na+].[OH-:28].[Ca+2].[OH-:30]>C1C=CC=CC=1.C(N(CC)CC)C>[OH:28][CH2:1]/[C:2](=[CH:3]\[CH2:4][CH2:5][CH:6]([CH2:8][CH2:9][OH:30])[CH3:7])/[CH3:10]Participants
7
Procedure
Prod.: (many methods) e.g. from Myrcene, via Myrcene dihydrochloride to Dichloro di-methyloctene. This is converted to Chloro di-hydrogeranyl acetate (andneryl acetate) with Sodium Acetate in Benzene in presence of Triethylamine. The acetates are saponified with Calcium hydroxide to yield Hydroxycitronellol, from which the aldehyde is prepared by oxidation.
Sources & evidence
- ORD record
- ord-7b27676bc8cf4c59a57c0fbff246c8fa
- Source dataset
- uspto-grants-1981_09
- Patent number
- US04287133
Reaction notes
Loading…