4-Trifluoromethyl-3-fluorobenzyl alcohol

4-Trifluoromethyl-3-fluorobenzyl alcohol Suppliers list
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Shanghai Harvest Chemical Industrial Co., Ltd.  
Tel: 15721252604 17321035817
Email: sales@harvest-chem.com
Company Name: Wuhan ariel chemical Co., LTD.  
Tel: 18986259541 18986259541
Email: sales@3stc.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Shanghai Worldyang Chemical Co.,Ltd.  
Tel: 021-56795766
Email: sales@worldyachem.com
4-Trifluoromethyl-3-fluorobenzyl alcohol Basic information
Product Name:4-Trifluoromethyl-3-fluorobenzyl alcohol
Synonyms:3-Fluoro-4-(trifluoromethyl)benzenemethanol;2-Fluoro-4-(hydroxymethyl)benzotrifluoride, [3-Fluoro-4-(trifluoromethyl)phenyl]methanol;3-Fluoro-4-(trifluoromethyl)benzylalcohol97%;(3-Fluoro-4-(trifluoromethyl)phenyl)methanol;4-Trifluoromethyl-3-fluorob;Benzenemethanol, 3-fluoro-4-(trifluoromethyl)-;(3-Fluoro-4-(trifluoromethyl)phenyl)meth
CAS:230295-16-6
MF:C8H6F4O
MW:194.13
EINECS:
Product Categories:Fluorine series
Mol File:230295-16-6.mol
4-Trifluoromethyl-3-fluorobenzyl alcohol Structure
4-Trifluoromethyl-3-fluorobenzyl alcohol Chemical Properties
Melting point 28-32°C
Boiling point 209℃
density 1.377
Fp 80℃
storage temp. Sealed in dry,Room Temperature
pka13.76±0.10(Predicted)
AppearanceLight green to green Solid-liquid mixture
CAS DataBase Reference230295-16-6
Safety Information
HS Code 2906290090
MSDS Information
4-Trifluoromethyl-3-fluorobenzyl alcohol Usage And Synthesis
Synthesis
3-FLUORO-4-(TRIFLUOROMETHYL)BENZALDEHYDE

204339-72-0

4-Trifluoromethyl-3-fluorobenzyl alcohol

230295-16-6

Step A: Preparation of (3-fluoro-4-(trifluoromethyl)phenyl)methanol: 3-fluoro-4-(trifluoromethyl)benzaldehyde (2.0 g, 10 mmol) and anhydrous methanol (20 mL) were added to a round-bottomed flask fitted with stirring bar. The flask was cooled in an ice bath, followed by the addition of sodium borohydride (0.47 g, 12 mmol) in batches. The ice bath was removed and the reaction mixture was allowed to warm naturally to room temperature. Saturated ammonium chloride solution (2 mL) was added and the mixture was subsequently concentrated under vacuum. The residue was diluted with additional saturated ammonium chloride solution (30 mL) and extracted with ethyl acetate (3 x 30 mL). The organic phases were combined, dried over magnesium sulfate, filtered and concentrated. Yield: 1.8 g (80%). The resulting product was used in the next reaction without further purification.

References[1] Patent: WO2014/78331, 2014, A1. Location in patent: Paragraph 00855
4-Trifluoromethyl-3-fluorobenzyl alcohol Preparation Products And Raw materials
Raw materials3-Fluoro-4-(trifluoromethyl)benzaldehyde-->Sodium borohydride-->Methanol
Tag:4-Trifluoromethyl-3-fluorobenzyl alcohol(230295-16-6) Related Product Information
4-Trifluoromethyl-3-fluorobenzyl alcohol 3-Fluoro-4-(trifluoromethyl)benzoic acid 2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzyl alcohol 2,3-Difluoro-4-(trifluoromethyl)benzoic acid 2,3,5,6-Tetrafluoro-4-(trifluoromethyl)benzoic acid 2,5-Difluoro-4-(trifluoromethyl)benzoic acid 3,5-Difluoro-4-(trifluoromethyl)benzoic acid RARECHEM AL BI 0450 RARECHEM AL BI 0529 RARECHEM AL BF 0450 RARECHEM AL BF 0529 2,3,6-TRIFLUORO-4-(TRIFLUOROMETHYL)BENZOIC ACID RARECHEM AL BD 0525 RARECHEM AL BF 0448 2,3-DIFLUORO-4-(TRIFLUOROMETHYL)BENZYL ALCOHOL RARECHEM AL BI 0448 RARECHEM AL BI 0525 6-Chloro-2,3-difluoro-4-(trifluoromethyl)benzoic acid