Hydrochloric Acid → 2-Methyl-6-methylene-7-octen-2-ol
Reaction equation
[CH3:1][C:2]1([CH3:11])[O:4][CH:3]1[CH2:5][CH2:6][C:7]([CH:9]=[CH2:10])=[CH2:8].CC(C)=CCCC(C=C)=C.Cl>>[CH3:11][C:2]([OH:4])([CH2:3][CH2:5][CH2:6][C:7]([CH:9]=[CH2:10])=[CH2:8])[CH3:1]Participants
4
Procedure
76 g. of epoxymyrcene, prepared according to the method described in paragraph a) by epoxidation of myrcene, were added dropwise between -5° and 0°, with good stirring. Then the mixture was stirred with 200 ml. ice-water and neutralised with diluted HCl. Following the same isolation procedure described in paragraph b) 1. the sec.-myrcenol was obtained with a comparable yield.
Workup
- additionwere added dropwise between -5° and 0°, with good stirring
Sources & evidence
- ORD record
- ord-9426bac87e4c43bebe9b9df9057c6ef0
- Source dataset
- uspto-grants-1976_06
- Patent number
- US03963783
Reaction notes
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