3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96
3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Basic information
- Product Name:
- 3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96
- Synonyms:
-
- 3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96
- 3-oxo-cyclohexanecarboxylic acid
- 3-Ketocyclohexyl carboxylate
- 3-Carboxycyclohexan-1-one
- 3-oxocyclohexanecarboxylate
- Cyclohexanecarboxylic acid, 3-oxo-
- 1-Carboxy-3-oxocyclohexane
- O**3-OXO-1-CYCLOHEXANECARBOXYLIC ACID
- CAS:
- 16205-98-4
- MF:
- C7H10O3
- MW:
- 142.15
- Product Categories:
-
- Carboxylic Acids
- Carboxylic Acids
- Ring Systems
- C7
- Carbonyl Compounds
- Mol File:
- 16205-98-4.mol
3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Chemical Properties
- Melting point:
- 76 °C
- Boiling point:
- 309.7±35.0 °C(Predicted)
- Density
- 1.233±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- solid
- pka
- 4.72±0.20(Predicted)
- color
- White
- InChI
- InChI=1S/C7H10O3/c8-6-3-1-2-5(4-6)7(9)10/h5H,1-4H2,(H,9,10)
- InChIKey
- WATQNARHYZXAGY-UHFFFAOYSA-N
- SMILES
- C1(C(O)=O)CCCC(=O)C1
3-OXO-1-CYCLOHEXANECARBOXYLIC ACID 96 Usage And Synthesis
Uses
3-Oxo-1-cyclohexanecarboxylic acid (3-oxocyclohexanecarboxylic acid) may be used in the preparation of 9-(4-chlorobenzoyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-2-carboxylic acid by reacting with 4-chloro-N-(4-methoxyphenyl)benzohydrazide hydrochloride via Fischer indolization.
General Description
3-Oxo-1-cyclohexanecarboxylic acid is a cyclic keto acid that can be prepared starting from 2-acetoxy-1,4-ethoxycarbonylcyclohex-1-ne.
Synthesis
606488-94-2
16205-98-4
Preparation of Jones oxidizing reagent: Jones reagent was prepared by mixing sulfuric acid (30 mL), CrO3 (8.1 g) and H2O (30 mL) under ice/water bath conditions. The prepared Jones reagent was slowly added dropwise to a solution of 3-hydroxycyclohexane-1-carboxylic acid (11 g, 76.3 mmol, 1.00 eq.) in acetone (150 mL) over 30 min at 0 °C. After the dropwise addition was completed, the reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the solid impurities were removed by filtration. The filtrate was extracted with dichloromethane (3 x 100 mL). The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the crude 3-oxocyclohexane-1-carboxylic acid (8.7 g) as a yellow oil.
References
[1] Patent: WO2014/11902, 2014, A1. Location in patent: Paragraph 00282-00283
[2] Patent: WO2014/194242, 2014, A2. Location in patent: Paragraph 00353; 00355
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