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85977-52-2

85977-52-2 Structure

85977-52-2 Structure
IdentificationMore
[Name]

(S)-(-)-1,2,3,4-Tetrahedro-naphthoic acid
[CAS]

85977-52-2
[Synonyms]

(s)-(-)-1,2,3,4-tetrahedro-naphthoic acid
(S)-1,2,3,4-TETRAHYDRO-NAPHTHALENE-1-CARBOXYLIC ACID
(S)-(-)-1,2,3,4-TETRAHYDRONAPHTHOIC ACID
(S)-1,2,3,4-TETRAHYDRO-NAPHTHOIC ACID
(S)-1,2,3,4-tetrahydro-1-naphthoic acid
(S)-(-)-1,2,3,4-Tetrahedro-1-NaphthoicAcid
(S)-1,2,3,4-TETRAHUDRO-1-NAPHTHOIC ACID
(S)-1,2,3,4-tetrahydro-1-naphtoic Acid
[Molecular Formula]

C11H12O2
[MDL Number]

MFCD07368365
[Molecular Weight]

176.21
[MOL File]

85977-52-2.mol
Chemical PropertiesBack Directory
[Melting point ]

54-56°C
[Boiling point ]

54-56°C
[density ]

1.186±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

Chloroform
[form ]

Solid
[pka]

4.28±0.20(Predicted)
[color ]

White
[InChI]

InChI=1S/C11H12O2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-2,4,6,10H,3,5,7H2,(H,12,13)/t10-/m0/s1
[InChIKey]

VDLWTJCSPSUGOA-JTQLQIEISA-N
[SMILES]

[C@@H]1(C(O)=O)C2=C(C=CC=C2)CCC1
[CAS DataBase Reference]

85977-52-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

22-36-51
[Safety Statements ]

26-24/25
[HS Code ]

29163990
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl acetate-->Methanol-->Tetrahydrofuran-->Petroleum ether-->Acetone-->Sodium borohydride-->Magnesium-->Carbon dioxide-->Phosphorus tribromide-->Dimethyl carbonate-->1-Tetralone-->QUININE SULFATE-->Cinchonine-->1,2,3,4-Tetrahydro-1-naphthoic acid
Hazard InformationBack Directory
[Chemical Properties]

White Solid
[Uses]

Intermediate in the preparation of Dipeptidyl Boronate Proteasome Inhibitors.
[Synthesis]

1,2,3,4-Tetrahydro-1-naphthoic acid

1914-65-4

(S)-(-)-1,2,3,4-Tetrahedro-naphthoic acid

85977-52-2

General procedure for the synthesis of (S)-tetrahydronaphthalenecarboxylic acid from 1,2,3,4-tetrahydro-1-naphthalenecarboxylic acid: 15.6 g (0.1 mol) of 1,2,3,4-tetrahydronaphthalenecarboxylic acid and 29.8 g (0.1 mol) of quinine were added to 158 mL of a 50% (v/v) aqueous ethanol solution, and stirred for 30 min at 50 °C until complete dissolution. The progress of the reaction was monitored by thin layer chromatography (TLC) with the unfolding agent ratio of petroleum ether (PE):ethyl acetate (EA) = 1:2. Upon completion of the reaction, the reaction solution was cooled to below 0 °C overnight to promote crystallization. Subsequent to filtration, the solid was collected and dried. The dried solid was recrystallized with 90 mL of ethanol, crystallized again at 0 °C, diafiltrated and dried. The resulting product was dissolved in a mixture of 55 mL of 1 mol/L hydrochloric acid and 100 mL of ethyl acetate in a partitioning operation. The organic phase was dried and filtered and concentrated to obtain the crude product. Finally, the crude product was recrystallized from hexane to give 7.21 g of (S)-1,2,3,4-tetrahydronaphthalenecarboxylic acid in the form of white solid in 43.6% yield.

[References]

[1] Patent: CN108084176, 2018, A. Location in patent: Paragraph 0093; 0102; 0103; 0104
[2] Arkiv foer Kemi, 1958, vol. 12, p. 161,165
[3] Patent: CN107382697, 2017, A
Spectrum DetailBack Directory
[Spectrum Detail]

(S)-(-)-1,2,3,4-Tetrahedro-naphthoic acid(85977-52-2)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

(S)-1,2,3,4-Tetrahydro-1-naphthoic acid, 98%(85977-52-2)
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93-09-4 16874-33-2 119-64-2 86-55-5 529-34-0 119904-90-4 23357-47-3 4242-18-6 1914-65-4 57576-44-0 85977-52-2