Boron tribromide → HCID 24949875, compound
Reaction equation
C[O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:13]3[CH:18]=[C:17]([CH3:19])[CH:16]=[C:15]([O:20]C)[CH:14]=3)[CH:9]=2)[CH:4]=1.B(Br)(Br)Br>>[OH:20][C:15]1[CH:14]=[C:13]([C:8]2[CH:9]=[C:10]3[C:5](=[CH:6][CH:7]=2)[CH:4]=[C:3]([OH:2])[CH:12]=[CH:11]3)[CH:18]=[C:17]([CH3:19])[CH:16]=1Participants
3
Procedure
The compound is prepared by reaction of 2-methoxy-6-(3-methoxy-5-methylphenyl)naphthalene (26 mg, 0.10 mmol, 1 eq) with boron tribromide solution (1 ml, 1 mmol, 10 eq) according to method G. After the processing, the analytically pure compound was obtained (quantitative yield, 25 mg).
Workup
- customAfter the processing, the analytically pure compound was obtained (quantitative yield, 25 mg)
Sources & evidence
- ORD record
- ord-403c808e41ba45fcb656c2dbddafcfd3
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08546392B2
Reaction notes
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