Sulfuric Acid → HCID 53701357, compound
Reaction equation
[CH2:1]([O:3][C:4]1[CH:9]=[C:8]([C@@H:10]2[CH2:15][CH:14]=[CH:13][CH2:12][C@H:11]2[N+:16]([O-:18])=[O:17])[CH:7]=[CH:6][C:5]=1[O:19][CH3:20])[CH3:2].[OH-].[K+].S(=O)(=O)(O)O>C(O)C>[CH2:1]([O:3][C:4]1[CH:9]=[C:8]([C@@H:10]2[CH2:15][CH:14]=[CH:13][CH2:12][C@@H:11]2[N+:16]([O-:18])=[O:17])[CH:7]=[CH:6][C:5]=1[O:19][CH3:20])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
89.25 g of (+/−)-trans-2-ethoxy-1-methoxy-4-(2-nitrocyclohex-4-enyl)benzene (compound D1) and 37 g of potassium hydroxide are dissolved in 500 ml of absolute ethanol. A solution of 23.5 ml of conc. sulfuric acid in 120 ml of absolute ethanol is then added dropwise such that the internal temperature does not exceed −2° C. After stirring for 1 h, the mixture is added to 4 l of ice water, and the precipitate is filtered off with suction, washed with water and dried. M.p. 66-67° C.
Workup
- customdoes not exceed −2° C
- filtrationthe precipitate is filtered off with suction
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-75f7b94b5b6e4879a6b3fc34ca09e1da
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06476025B1
Reaction notes
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