Benzyl Chloride → HCID 20498267, compound
Reaction equation
[CH2:1]([O:3][CH2:4][CH2:5][O:6][CH2:7][CH:8]1[O:13][CH2:12][CH:11]([OH:14])[CH2:10][CH2:9]1)[CH3:2].[CH2:15](Cl)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH2:1]([O:3][CH2:4][CH2:5][O:6][CH2:7][CH:8]1[CH2:9][CH2:10][CH:11]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:12][O:13]1)[CH3:2]Participants
3
Procedure
5 was prepared as a liquid, boiling point not determined, by treating 5B with benzyl chloride according to the procedure described in the last paragraph of Example 1.
Workup
- custom5 was prepared as a liquid
Sources & evidence
- ORD record
- ord-eba04b31c594416fa049ac4009d9608b
- Source dataset
- uspto-grants-1983_06
- Patent number
- US04388104
Reaction notes
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