| Identification | Back Directory | [Name]
4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE | [CAS]
3470-46-0 | [Synonyms]
2-Carboxy-5-oxo-5,6,7,8-tetrahydronaphthalene 5-Oxo-7,8-dihydro-6H-naphthalene-2-carboxylic Acid 4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE 4-[(4-METHYLPHENYL)SULPHONYL]PIPERIDINE HYDROCHLORIDE 2-Naphthalenecarboxylic acid, 5,6,7,8-tetrahydro-5-oxo- 5-Oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid 96% 6-Carboxy-1-oxo-1,2,3,4-tetrahydronaphthalene, 5-Oxo-5,6,7,8-tetrahydro-2-naphthoic acid | [Molecular Formula]
C11H10O3 | [MDL Number]
MFCD04039168 | [MOL File]
3470-46-0.mol | [Molecular Weight]
190.2 |
| Chemical Properties | Back Directory | [Melting point ]
230(dec.) | [Boiling point ]
230 °C/dec) | [density ]
1.309±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
solid | [pka]
3.77±0.20(Predicted) | [color ]
Light brown |
| Hazard Information | Back Directory | [Synthesis]
Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate (320 mg, 1.57 mmol) was used as a raw material and dissolved in a solvent mixture of 6 mL of methanol and 3 mL of water. Subsequently, lithium hydroxide (331 mg, 7.88 mmol) was added. The reaction mixture was stirred at room temperature for 1 h. The progress of the reaction was monitored by thin-layer chromatography (TLC), and after confirming that the reaction was complete, the pH of the reaction solution was adjusted to 5 with 1 N hydrochloric acid solution.The reaction solution was concentrated by rotary evaporation and extracted with ethyl acetate (50 mL × 2). The ethyl acetate extracts were combined and the solvent was removed by rotary evaporation to afford the white solid product 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid (310 mg, 100% yield). | [References]
[1] Patent: CN104844471, 2017, B. Location in patent: Paragraph 0186; 0187; 0188 |
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