1-Bromopropane → p-[(1,5-Dimethyl-hexyl)-oxy]-alpha-propoxy-toluene
Reaction equation
[CH3:1][CH:2]([O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][OH:15])=[CH:12][CH:11]=1)[CH2:3][CH2:4][CH2:5][CH:6]([CH3:8])[CH3:7].[CH2:18](Br)[CH2:19][CH3:20]>>[CH3:1][CH:2]([O:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][O:15][CH2:18][CH2:19][CH3:20])=[CH:12][CH:11]=1)[CH2:3][CH2:4][CH2:5][CH:6]([CH3:7])[CH3:8]Participants
3
Procedure
By the process described in Example 1, p-[(1,5-dimethyl-hexyl)-oxy]-benzyl alcohol is reacted with propyl bromide to give p-[(1,5-dimethyl-hexyl)-oxy]-α-propoxy-toluene (boiling point = 198°-200° C/1.0 mmHg).
Sources & evidence
- ORD record
- ord-fe4471cf52dc4e718b53dc0076aae04f
- Source dataset
- uspto-grants-1977_01
- Patent number
- US04001339
Reaction notes
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