Benzyl Chloride → 5,7-Dimethyl-4-(phenylmethoxy)-6,8-dioxabicyclo(3.2.1)octane
Reaction equation
[CH3:1][C:2]12[O:10][CH:6]([CH:7]([CH3:9])[O:8]1)[CH2:5][CH2:4][CH:3]2[OH:11].[CH2:12](Cl)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.O1CCCC(O)C1>>[CH3:1][C:2]12[O:10][CH:6]([CH:7]([CH3:9])[O:8]1)[CH2:5][CH2:4][CH:3]2[O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
4
Procedure
18A was treated with benzyl chloride, by the procedure described for treatment of 1A, to give 18, as a liquid, b.p.: 145° C., 0.06 Torr.
Sources & evidence
- ORD record
- ord-1d636fc600564aad82c6dc544f985167
- Source dataset
- uspto-grants-1983_06
- Patent number
- US04388104
Reaction notes
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