Isopropanol → HCID 15392240, compound
Reaction equation
[CH:1]([C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][C:9]([C:13]#[N:14])=[CH:10]2)=[CH:5][CH:4]=1)=[O:2].C([OH:18])(C)C>CC(C)=O.S(=O)(=O)(O)O.O.[O-2].[Cr+3].[O-2].[O-2].[Cr+3]>[C:13]([C:9]1[CH:10]=[C:11]2[C:6]([CH:5]=[CH:4][C:3]([C:1]([OH:18])=[O:2])=[CH:12]2)=[CH:7][CH:8]=1)#[N:14]Participants
Conditions
- Temperature
- 0 °C
Procedure
7-Formyl-2-naphthalenecarbonitrile obtained in Reference Example 1 (3.0 g) was dissolved in 50 ml of acetone. The solution was cooled to 0° C. with stirring, and a solution prepared by dissolving 10 g of chromium oxide (IV) in 11 ml of concentrated sulfuric acid and 50 ml of water was added until the mixture becomes orange yellow. The reaction solution was stirred at 0° C. for 90 minutes and then at room temperature for 45 minutes, followed by the addition of 2 ml of isopropyl alcohol. The reaction solution was evaporated, water was added to the resulting residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was extracted with saturated sodium bicarbonate aqueous solution, the saturated sodium bicarbonate layer was adjusted to pH 1 by adding concentrated sulfuric acid, and the thus precipitated solid matter was collected by filtration to give 1.94 g of 7-cyano-2-naphthalenecarboxylic acid.
Workup
- customa solution prepared
- additionwas added until the mixture
- stirringThe reaction solution was stirred at 0° C. for 90 minutes
- customThe reaction solution was evaporated
- additionwater was added to the resulting residue
- extractionthe mixture was extracted with ethyl acetate
- extractionThe ethyl acetate layer was extracted with saturated sodium bicarbonate aqueous solution
- additionby adding concentrated sulfuric acid
- filtrationthe thus precipitated solid matter was collected by filtration
Sources & evidence
- ORD record
- ord-19c8a3c65b66472ba55f483feab10180
- Source dataset
- uspto-grants-1999_02
- Patent number
- US05869501
Reaction notes
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