Hydrochloric Acid → (+/-)-cis1,2-Dimethoxy-4-(2-nitrocyclohexyl)benzene
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH:13]=[CH:12][CH2:11][C@@H:10]2[N+:15]([O-:17])=[O:16])=[CH:5][C:4]=1[O:18][CH3:19].Cl>CO.[Pd]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH2:13][CH2:12][CH2:11][C@@H:10]2[N+:15]([O-:17])=[O:16])=[CH:5][C:4]=1[O:18][CH3:19]Participants
5
Procedure
8.4 g of (+/−)-cis-1,2-dimethoxy-4-(2-nitrocyclohex-4-enyl)benzene are dissolved in 450 ml of methanol, admixed with 2 ml of conc. hydrochloric acid and hydrogenated after the addition of 500 mg of Pd/C 10%. The reaction mixture is filtered and the filtrate is concentrated. M.p.: 84-86.5° C.; Yield quantitative.
Workup
- filtrationThe reaction mixture is filtered
- concentrationthe filtrate is concentrated
- customYield quantitative
Sources & evidence
- ORD record
- ord-ae2a2b456cf045cd831f4e13685feabc
- Source dataset
- uspto-grants-2001_02
- Patent number
- US06191138B1
Reaction notes
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