HCID 514300, compound → HCID 70625137, compound
Reaction equation
[CH2:1]([C:3](=[CH:12][CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]2[O:21][CH2:22][O:23][C:17]=2[CH:16]=1)[CH2:4][CH2:5][CH:6]1[CH2:10][CH2:9][CH2:8][C:7]1=[O:11])[CH3:2].[CH2:24]([Mg]Br)[CH3:25]>>[CH2:24]([C:7]1([OH:11])[CH2:8][CH2:9][CH2:10][CH:6]1[CH2:5][CH2:4][C:3]([CH2:1][CH3:2])=[CH:12][CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][C:18]2[O:21][CH2:22][O:23][C:17]=2[CH:16]=1)[CH3:25]Participants
3
Procedure
2-[3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]-cyclopentanone can be treated with ethylmagnesium bromide according to the procedure of Example 2, part (c) to give 1-ethyl-2-[3-ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]cyclopentanol [XV; Ar is 3,4-methylenedioxyphenyl, Y is C(C2H5)=CHCH2CH2, R' is C2H5, m is 1. ].
Sources & evidence
- ORD record
- ord-567d55e433bf4f9f941e1516aa228502
- Source dataset
- uspto-grants-1978_11
- Patent number
- US04125541
Reaction notes
Loading…