Boron Trichloride → 89227-39-4
Reaction equation
C([O:8][C:9]1[C:10](=[O:30])[C:11]2[C:16]([C:17](=[O:27])[C:18]=1[O:19]CC1C=CC=CC=1)=[C:15]([C:28]#[N:29])[CH:14]=[CH:13][CH:12]=2)C1C=CC=CC=1.B(Cl)(Cl)Cl>>[OH:8][C:9]1[C:10](=[O:30])[C:11]2[C:16]([C:17](=[O:27])[C:18]=1[OH:19])=[C:15]([C:28]#[N:29])[CH:14]=[CH:13][CH:12]=2Participants
3
Procedure
Treatment of 2,3-dibenzyloxy-5-cyano-1,4-naphthoquinone with boron trichloride as in Preparation 15 above gives 2,3-dihydroxy-5-cyano-1,4-naphthoquinone, mp 305°-312°.
Sources & evidence
- ORD record
- ord-7c46211cc41b4a1ab3c63e24b01e2924
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04419368
Reaction notes
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