ChemicalBook--->CAS DataBase List--->3470-46-0

3470-46-0

3470-46-0 Structure

3470-46-0 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302+H312+H332-H314
[Precautionary statements ]

P301+P310-P309+P311
[Hazard Codes ]

Xi,C
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2902900000
Spectrum DetailBack Directory
[Spectrum Detail]

4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE(3470-46-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate

144464-66-4

4-[(4-METHYLPHENYL)SULFONYL]PIPERIDINE HYDROCHLORIDE

3470-46-0

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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