3-Nitrophenethyl alcohol

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Company Name: Amatek Scientific Co. Ltd.  Gold
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3-Nitrophenethyl alcohol manufacturers

3-Nitrophenethyl alcohol Basic information
Product Name:3-Nitrophenethyl alcohol
Synonyms:TIMTEC-BB SBB008558;2-(3-Nitrophenyl)ethanol;3-nitro-benzeneethano;3-Nitrobenzeneethanol;beta-(m-Nitrophenyl)ethanol;m-nitrophenethyl alcohol;3-Nitrophenylethylalcohol;2-(3-Nitrophnyl)ethanol
CAS:52022-77-2
MF:C8H9NO3
MW:167.16
EINECS:257-611-2
Product Categories:Alcohols;C7 to C8;Oxygen Compounds;Building Blocks;C7 to C8;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
Mol File:52022-77-2.mol
3-Nitrophenethyl alcohol Structure
3-Nitrophenethyl alcohol Chemical Properties
Melting point 47-50 °C (lit.)
Boiling point 141-146 °C/4 mmHg (lit.)
density 1.2917 (rough estimate)
refractive index 1.5570 (estimate)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
pka14.65±0.10(Predicted)
form solid
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C8H9NO3/c10-5-4-7-2-1-3-8(6-7)9(11)12/h1-3,6,10H,4-5H2
InChIKeyPWZWTSYUZQZFKE-UHFFFAOYSA-N
SMILESC1(CCO)=CC=CC([N+]([O-])=O)=C1
EPA Substance Registry SystemBenzeneethanol, 3-nitro- (52022-77-2)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39
WGK Germany 3
TSCA TSCA listed
HS Code 2906290090
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
3-Nitrophenethyl alcohol Usage And Synthesis
Uses3-Nitrophenethyl alcohol has been employed as substrate to engineer nitrobenzene dioxygenase for the production of the highly potent antioxidant, hydroxytyrosol.
Synthesis
3-NITROPHENYLACETIC ACID

1877-73-2

3-NITROPHENETHYL ALCOHOL

52022-77-2

Under nitrogen protection, 200 mg of 3-nitrophenylacetic acid was dissolved in 2 mL of anhydrous tetrahydrofuran and 1 mL of borane-tetrahydrofuran solution (1 M) was added slowly and dropwise. The reaction mixture was stirred at room temperature for 12 h, during which the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, a small amount of water was carefully added dropwise to quench the reaction. Subsequently, the reaction system was adjusted to alkaline by adding excess saturated sodium bicarbonate solution. Extraction was carried out with ethyl acetate and the organic layer was separated, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give the crude product. Finally, purification by column chromatography afforded 125 mg of 3-nitrophenylethanol (Intermediate XVI) in 68% yield.

References[1] Patent: CN103787992, 2016, B. Location in patent: Paragraph 0309-0312
[2] Patent: WO2014/182829, 2014, A1. Location in patent: Page/Page column 55
[3] Patent: WO2016/191172, 2016, A1. Location in patent: Page/Page column 78
[4] Helvetica Chimica Acta, 1973, vol. 56, p. 2460 - 2479
[5] Journal of the American Chemical Society, 1982, vol. 104, # 7, p. 1937 - 1951
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