4-Chlororesorcinol → HCID 58913587, compound
Reaction equation
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([OH:6])=[CH:4][C:3]=1[OH:9].[CH3:10][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:18][C:19]([OH:21])=O.P(Cl)(Cl)(Cl)(Cl)Cl.[CH3:28]N(C=O)C>>[Cl:1][C:2]1[CH:8]=[C:7]2[C:5](=[CH:4][C:3]=1[OH:9])[O:6][CH:28]=[C:18]([C:13]1[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=1[O:11][CH3:10])[C:19]2=[O:21]Participants
5
Procedure
This compounds was synthesised in the same manner as described above. 4-Chlororesorcinol (1.74 g, 12.0 mmol), 2-methoxyphenylacetic acid (2.0 g, 12.0 mmol), BF3Et2O (10 ml), PCl5 (3.76 g, 18.1 mmol), DMF (20 ml and 10 ml). The pale brown solid precipitate was taken directly onto the next stage without further purification.
Workup
- customThis compounds was synthesised in the same manner
- customThe pale brown solid precipitate was taken directly onto the next stage without further purification
Sources & evidence
- ORD record
- ord-c87310f3a2124578ae00ff562c387848
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07247734B2
Reaction notes
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