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503315-74-0

503315-74-0 Structure

503315-74-0 Structure
IdentificationBack Directory
[Name]

3-Fluoro-4-nitrobenzyl alcohol 99%
[CAS]

503315-74-0
[Synonyms]

Structure
(3-Fluoro-4-nitrophenyl)
3-Fluoro-4-nitrobenzenemethanol
3-Fluoro-4-nitrobenzylalcohol98%
Benzenemethanol, 3-fluoro-4-nitro-
3-Fluoro-4-nitrobenzyl alcohol 99%
(3-Fluoro-4-nitrophenyl)methanol, 2-Fluoro-4-(hydroxymethyl)nitrobenzene
[Molecular Formula]

C7H6FNO3
[MDL Number]

MFCD03094236
[MOL File]

503315-74-0.mol
[Molecular Weight]

171.13
Chemical PropertiesBack Directory
[Boiling point ]

328.6±27.0 °C(Predicted)
[density ]

1.434
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Solid
[pka]

13.27±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Warning
[Hazard statements ]

H302-H361
[Precautionary statements ]

P201-P202-P264-P270-P281-P301+P312-P308+P313-P330-P405-P501
[HS Code ]

2906290090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Fluoro-4-nitrobenzyl alcohol 99%(503315-74-0)1HNMR
3-Fluoro-4-nitrobenzyl alcohol 99%(503315-74-0)1HNMR
3-Fluoro-4-nitrobenzyl alcohol 99%(503315-74-0)19FNMR
3-Fluoro-4-nitrobenzyl alcohol 99%(503315-74-0)13CNMR
Hazard InformationBack Directory
[Synthesis]

3-Fluoro-4-nitrobenzoic acid

403-21-4

3-Fluoro-4-nitrobenzyl alcohol  99%

503315-74-0

Part A. Preparation of (3-fluoro-4-nitrophenyl)methanol. To a solution of 3-fluoro-4-nitrobenzoic acid (2.0 g, 10.8 mmol) in tetrahydrofuran (THF, 50 ml) was added dropwise borane-dimethyl sulfide complex (BH3-Me2S, 2.215 ml, 22.15 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 3 h, followed by warming up to 65 °C and continued stirring for 18 h. The reaction was carried out at 0 °C. Upon completion of the reaction, the mixture was cooled to room temperature and the reaction was quenched by the slow addition of ice (50 g) followed by the addition of 1 M aqueous hydrochloric acid solution (100 ml). The reaction mixture was extracted with ethyl acetate (EtOAc, 200 ml), the organic layers were combined, dried over anhydrous sodium sulfate (Na2SO4), filtered and concentrated under reduced pressure to give the title compound (3-fluoro-4-nitrophenyl)methanol as a white solid (1.79 g, 97% yield).

[References]

[1] Patent: WO2009/39135, 2009, A1. Location in patent: Page/Page column 140
[2] Journal of Medicinal Chemistry, 2018, vol. 61, # 3, p. 1153 - 1163
[3] Patent: WO2011/66416, 2011, A1. Location in patent: Page/Page column 16
[4] Patent: WO2004/7491, 2004, A1. Location in patent: Page 65
[5] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 13, p. 3986 - 3991
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