1-Naphthol → HCID 13136910, compound
Reaction equation
[C:1]1([OH:11])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.Cl.O=[C:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH:15]1[C:20](O)=[O:21]>>[CH2:16]1[C:15]2[C:20](=[O:21])[O:11][C:1]3[C:10]4[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=4)[CH:4]=[CH:3][C:2]=3[C:14]=2[CH2:19][CH2:18][NH:17]1Participants
3
Procedure
Prepared by the method described in Example 1 from 1-napthol (10.0 g, 0.069 moles) and 4-oxo-3-piperidinecarboxylate hydrochloride (9.6 g, 0.05 moles). Recrystallization from 2-propanol/N,N-dimethylformamide yielded the product (3.7 g), mp 227°-230° C.
Workup
- customPrepared by the method
- customRecrystallization from 2-propanol/N,N-dimethylformamide
Sources & evidence
- ORD record
- ord-6eec5184ef1647428e1581cbe2c0c276
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04382939
Reaction notes
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