Myrcene → (Z)-2,6-dimethyloct-2-ene-1,8-diol

HRID 1577075Notes

Reaction equation

HRID 1577075 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

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