ChemicalBook > Product Catalog >Organic Chemistry >Alcohols,Phenols,Phenol alcohols >cyclitols >4-Fluoro-3-hydroxybenzyl alcohol

4-Fluoro-3-hydroxybenzyl alcohol

4-Fluoro-3-hydroxybenzyl alcohol Suppliers list
Company Name: Amadis Chemical Company Limited  
Tel: 571-89925085
Email: sales@amadischem.com
Company Name: AAB-PHARMA LIMITED  
Tel: 025-66800956 18800000000
Email: sales@njdmchem.com
Company Name: Shanghai Jizhi Biochemical Technology Co. Ltd.  
Tel: 021-4009004166/18616739031 18616739031
Email: 3007523370@qq.com
Company Name: Suzhou Rovathin Foreign Trade Co.,Ltd  
Tel: 0512-65816829 18662214788
Email: info@rovathin.com.cn
Company Name: Henan Pusai Chemical Products Co., Ltd.  
Tel: 0371-63357898
Email: 1280786222@qq.com
4-Fluoro-3-hydroxybenzyl alcohol Basic information
Product Name:4-Fluoro-3-hydroxybenzyl alcohol
Synonyms:4-Fluoro-3-hydroxybenzyl alcohol;2-Fluoro-5-(hydroxymethyl)phenol;2-Fluoro-5-(hydroxymethyl)phenol 95+%;Benzenemethanol, 4-fluoro-3-hydroxy-
CAS:934241-78-8
MF:C7H7FO2
MW:142.13
EINECS:
Product Categories:
Mol File:934241-78-8.mol
4-Fluoro-3-hydroxybenzyl alcohol Structure
4-Fluoro-3-hydroxybenzyl alcohol Chemical Properties
Boiling point 272.4±25.0 °C(Predicted)
density 1.342±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka8.49±0.10(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2908190090
MSDS Information
4-Fluoro-3-hydroxybenzyl alcohol Usage And Synthesis
Synthesis
METHYL 4-FLUORO-3-HYDROXYBENZOATE

214822-96-5

4-Fluoro-3-hydroxybenzyl alcohol

934241-78-8

The general procedure for the synthesis of 4-fluoro-3-hydroxybenzyl alcohol from methyl 4-fluoro-3-hydroxybenzoate was as follows: LiBH4 (2.37 g, 109 mmol) was suspended in THF (50 mL) at room temperature, followed by the addition of methyl 4-fluoro-3-hydroxybenzoate (5.0 g, 27.2 mmol). The reaction mixture was stirred under reflux conditions for 24 hours. After completion of the reaction, the mixture was concentrated. The residue was partitioned between EtOAc (100 mL) and 1N HCl (100 mL). The aqueous layer was extracted with EtOAc (50 mL × 2) and the combined organic layers were washed with brine, dried over MgSO4 and concentrated. The residue was purified by fast column chromatography to afford 4-fluoro-3-hydroxybenzyl alcohol (2.76 g, 19.4 mmol, 66% yield) as a white solid.1H NMR (CDCl3) δ: 7.09-7.00 (2H, m), 6.88-6.82 (1H, m), 5.24 (1H, d, J = 4.0 Hz), 4.60 (2H, s) , 1.68 (1H, brs).

References[1] Patent: US2011/136801, 2011, A1. Location in patent: Page/Page column 64
4-Fluoro-3-hydroxybenzyl alcohol Preparation Products And Raw materials
Raw materialsMethyl 4-fluoro-3-hydroxybenzoate-->Lithium borohydride-->Tetrahydrofuran
Tag:4-Fluoro-3-hydroxybenzyl alcohol(934241-78-8) Related Product Information
4-Fluoro-3-methoxybenzyl alcohol 4-Fluoro-3-hydroxybenzoic acid 4-fluoro-3-hydroxy-benzaldehyde Methyl 4-fluoro-3-hydroxybenzoate 3-fluoro-5-(hydroxymethyl)phenol 4-Fluoro-3-(phenylmethoxy)benzenemethanol