Potassium Hydroxide → HCID 12138719, compound
Reaction equation
[OH-].[K+].[O:3]1[C:8]2[CH:9]=[CH:10][C:11]([CH:13]=[O:14])=[CH:12][C:7]=2[O:6][CH2:5][CH2:4]1.[N+:15]([CH2:17][C:18]([N:20]1[CH2:24][CH2:23][CH2:22][CH2:21]1)=[O:19])#[C-:16]>CO>[O:3]1[C:8]2[CH:9]=[CH:10][C:11]([C@@H:13]3[O:14][CH:16]=[N:15][C@H:17]3[C:18]([N:20]3[CH2:24][CH2:23][CH2:22][CH2:21]3)=[O:19])=[CH:12][C:7]=2[O:6][CH2:5][CH2:4]1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred and cooled (0° C.) solution of potassium hydroxide (2.70 g, 48.1 mmol) in methanol (30 ml) was added a mixture of 1,4-benzodioxan-6-carboxaldehyde (8.20 g, 50.0 mmol) and the product from Example 1 (6.30 g, 45.6 mmol). The solution was stirred overnight with continued cooling and then concentrated. The residue was partitioned between ethyl acetate and water. The organic layer was combined with additional ethyl acetate extracts, washed with aqueous sodium chloride and dried (magnesium sulfate). Concentration afforded crude product as a golden, glassy solid. Flash chromatography over silica (ethyl acetate) yielded 9.40 g (68%) of product as a colorless glassy solid. 1H NMR (CDCl3) δ 6.99 (s, 1H), 6.90–6.78 (m, 3H), 6.00 (d, J=7.3, 1H), 4.58, (d, J=7.3, 1H), 4.26 (s, 4H), 3.95–3.87 (m, 1H), 3.55–3.41 (m, 3H), 2.04–1.80 (m, 4H) ppm.
Workup
- additionwas added
- stirringThe solution was stirred overnight
- temperaturewith continued cooling
- concentrationconcentrated
- customThe residue was partitioned between ethyl acetate and water
- washwashed with aqueous sodium chloride
- dry with materialdried (magnesium sulfate)
- concentrationConcentration
- customafforded crude product as a golden, glassy solid
Sources & evidence
- ORD record
- ord-757d94dc4ee14ffd82bc11e9936d2697
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07041831B2
Reaction notes
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