Butyl iodide → HCID 18476309, compound
Reaction equation
[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:3]=1[OH:17].[CH2:18](I)[CH2:19][CH2:20][CH3:21]>>[Br:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[C:4]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[C:3]=1[O:17][CH2:18][CH2:19][CH2:20][CH3:21]Participants
3
Procedure
The intermediate was prepared from ethyl 4-bromo-3-hydroxynaphthalen-2-carboxylate and butyl iodide in almost quantitative yield and used for the next step without further purification.
Workup
- customused for the next step without further purification
Sources & evidence
- ORD record
- ord-fa39e74398ad43b6a7cafd5b8eedb04f
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06410562B1
Reaction notes
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