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Ark Pharm, Inc. |
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847-367-3680 |
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sales@arkpharminc.com |
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| | 7-Hydroxy-1,2,3,4-tetrahydroquinoline Basic information |
| Product Name: | 7-Hydroxy-1,2,3,4-tetrahydroquinoline | | Synonyms: | 7-Hydroxy-1,2,3,4-Tetrahydro Quinolinoe;7-Hydroxy-1,2,3,4-tetrahydroquinoline;7-hydroxy-1,2,3,4-Tetrahydro-quinolin;1,2,3,4-Tetrahydro-quinolin-7-ol;1,2,3,4-Tetrahydro-7-quinolinol;7-Quinolinol, 1,2,3,4-tetrahydro-;7-Hydroxy-1,2,3,4-tetrahydroquinoL;7-Hydroxy-1,2,3,4-tetrahydroquinoline ISO 9001：2015 REACH | | CAS: | 58196-33-1 | | MF: | C9H11NO | | MW: | 149.19 | | EINECS: | | | Product Categories: | | | Mol File: | 58196-33-1.mol |  |
| | 7-Hydroxy-1,2,3,4-tetrahydroquinoline Chemical Properties |
| Melting point | 70-80 °C | | Boiling point | 319.7±31.0 °C(Predicted) | | density | 1.141±0.06 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | solubility | Chloroform (Sparingly), Methanol (Slightly) | | pka | 10.70±0.20(Predicted) | | form | Solid | | color | Dark Orange to Very Dark Orange | | Stability: | Light Sensitive | | InChI | InChI=1S/C9H11NO/c11-8-4-3-7-2-1-5-10-9(7)6-8/h3-4,6,10-11H,1-2,5H2 | | InChIKey | HJJRGZMJZDSMDB-UHFFFAOYSA-N | | SMILES | N1C2=C(C=CC(O)=C2)CCC1 | | CAS DataBase Reference | 58196-33-1(CAS DataBase Reference) | | EPA Substance Registry System | 7-Quinolinol, 1,2,3,4-tetrahydro- (58196-33-1) |
| WGK Germany | WGK 3 | | TSCA | TSCA listed | | HS Code | 2933499090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Acute Tox. 4 Oral |
| | 7-Hydroxy-1,2,3,4-tetrahydroquinoline Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of 7-hydroxy-1,2,3,4-tetrahydroquinoline from 3,4-dihydro-7-hydroxy-2(1H)-quinolinone was as follows: 7-hydroxy-3,4-dihydroquinolin-2(1H)-one (2.00 g, 12.26 mmol) was dissolved in tetrahydrofuran (THF, 20 mL) and the solution was cooled down to 0 °C. Subsequently, sodium borohydride (NaBH4, 1.07 g, 28.19 mmol) was added, and then iodine (I2, 3.42 g, 13.48 mmol) dissolved in THF (20 mL) was slowly added dropwise through the addition funnel to the reaction mixture. After installing the condenser, the reaction mixture was refluxed overnight. After completion of the reaction, the reaction mixture was neutralized with 3 M hydrochloric acid solution and then extracted three times with dichloromethane. The organic layers were combined and dried with anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give a viscous yellow oil. Finally, the crude product was purified by fast column chromatography to afford 7-hydroxy-1,2,3,4-tetrahydroquinoline as a white crystalline solid (1.80 g, 98% yield). | | References | [1] Angewandte Chemie - International Edition, 2013, vol. 52, # 2, p. 650 - 654
[2] Angew. Chem., 2013, vol. 125, # 2, p. 678 - 682,5
[3] Chinese Chemical Letters, 2018, vol. 29, # 10, p. 1497 - 1499
[4] Organic Letters, 2011, vol. 13, # 23, p. 6196 - 6199
[5] Organic and Biomolecular Chemistry, 2013, vol. 11, # 24, p. 3954 - 3962 |
| | 7-Hydroxy-1,2,3,4-tetrahydroquinoline Preparation Products And Raw materials |
| Raw materials | 3,4-Dihydro-7-hydroxy-2(1H)-quinolinone-->7-Methoxy-1,2,3,4-tetrahydroquinoline-->Sodium borohydride-->Tetrahydrofuran | | Preparation Products | 7-Methoxy-3,4-dihydro-1H-quinolin-2-one-->7-Hydroxyquinoline-->1-Ethyl-1,2,3,4-tetrahydroquinoline-7-ol-->7-Quinolinol, 1,2,3,4-tetrahydro-1-methyl- |
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