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4-Hydroxyindan-1-one

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4-Hydroxyindan-1-one Basic information
Product Name:4-Hydroxyindan-1-one
Synonyms:4-HYDROXY-1-INDANONE;4-HYDROXY-INDAN-1-ONE;4-HYDROXYINDANONE;Hydroxyindanone;2,3-dihydro-4-hydroxyinden-1-one;4-HYDROXYINDANONE 98+%;1H-Inden-1-one,2,3-dihydro-4-hydroxy-;4-Hydroxy-1-indanone,97%
CAS:40731-98-4
MF:C9H8O2
MW:148.16
EINECS:
Product Categories:Indanone & Indene;C9;Carbonyl Compounds;Ketones;Indane/Indanone and Derivatives
Mol File:40731-98-4.mol
4-Hydroxyindan-1-one Structure
4-Hydroxyindan-1-one Chemical Properties
Melting point 242-244 °C (lit.)
Boiling point 307.6±31.0 °C(Predicted)
density 1.305±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in ethanol. (25mg/ml)
form powder to crystal
pka9.22±0.20(Predicted)
color White to Orange to Green
InChIInChI=1S/C9H8O2/c10-8-3-1-2-6-7(8)4-5-9(6)11/h1-3,10H,4-5H2
InChIKeyCKSCMRNFDBWFND-UHFFFAOYSA-N
SMILESC1(=O)C2=C(C(O)=CC=C2)CC1
CAS DataBase Reference40731-98-4(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HS Code 29145090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
4-Hydroxyindan-1-one Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses4-Hydroxy-1-indanone is a hydroxylated indanone used for synthesis. It is an important raw material and intermediate used in Organic Synthesis, Pharmaceuticals, Agrochemicals and Dyestuffs.
Synthesis
Dihydrocoumarin

119-84-6

4-Hydroxyindan-1-one

40731-98-4

General procedure for the synthesis of 4-hydroxy-1-indanone from hydrogenated cinnamic acid lactone: A mixture of aluminum chloride (90.0 g, 676 mmol) and sodium chloride was stirred at 150 °C until the solid was completely dissolved, followed by the slow dropwise addition of hydrogenated cinnamic acid lactone (20.0 g, 135 mmol). After the dropwise addition, the reaction mixture was warmed to 200 °C and stirred continuously for 1 hour. Upon completion of the reaction, the mixture was cooled to room temperature and slowly poured into ice water (500 mL), followed by filtration to collect the crude product. The crude product was purified by recrystallization to afford 4-hydroxy-1-indanone (19 g, 95% yield) as a gray solid. The structure of the compound was confirmed by the following spectral data: mass spectrum (ESI positive ion mode) m/z 149.5 [M + H]+; 1H NMR (400 MHz, CDCl3) δ (ppm): 7.41-7.38 (m, 1H), 7.24-7.19 (m, 1H), 6.80-6.79 (m, 1H), 6.78-6.77 (d , 1H, J = 4.0 Hz), 5.46 (br, 1H), 3.06-3.03 (m, 2H), 2.69-2.66 (m, 2H).

References[1] Patent: WO2014/19344, 2014, A1. Location in patent: Paragraph 00820
[2] Patent: WO2014/82380, 2014, A1. Location in patent: Paragraph 00314; 00315
[3] Patent: WO2014/82379, 2014, A1. Location in patent: Page/Page column 112; 113
[4] Patent: WO2014/131315, 2014, A1. Location in patent: Page/Page column 112
[5] Patent: US2015/79028, 2015, A1. Location in patent: Paragraph 2389; 2390; 2391; 2392; 2393
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