1-(4-Chlorobutyl)-1-methyl-7-methoxy-2-tetralone → 1-(4-Chlorobutyl)-1-Ethyl-7-Methoxy-2-Tetralone
Reaction equation
[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1([CH3:19])[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:16][CH3:17])[CH:14]=2)[CH2:9][CH2:8][C:7]1=[O:18].[CH2:20](C1C2C(=CC=C(OC)C=2)CCC1=O)C>>[Cl:1][CH2:2][CH2:3][CH2:4][CH2:5][C:6]1([CH2:19][CH3:20])[C:15]2[C:10](=[CH:11][CH:12]=[C:13]([O:16][CH3:17])[CH:14]=2)[CH2:9][CH2:8][C:7]1=[O:18]Participants
3
Procedure
Using a procedure analogous to that described in Example I for the preparation of 1-(4-chlorobutyl)-1-methyl-7-methoxy-2-tetralone there is obtained from 35 g. of 1-ethyl-7-methoxy-2-tetralone; 37.4 g. of the title product b.p. 160°-173° C. (0.4 mm.). I. R. Analysis: 5.83, 8.0 μ.
Workup
- customthere is obtained from 35 g
Sources & evidence
- ORD record
- ord-1ffebdfad46c4f618463e4a7dd5591dc
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03931328
Reaction notes
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