3,5-Bis(trifluoromethyl)anisole

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3,5-Bis(trifluoromethyl)anisole manufacturers

3,5-Bis(trifluoromethyl)anisole Basic information
Product Name:3,5-Bis(trifluoromethyl)anisole
Synonyms:1-Methoxy-3,5-bis(trifluoromethyl)benzene;1,3-Bis(trifluoromethyl)-5-methoxybenzene, 3,5-Bis(trifluoromethyl)phenyl methyl ether;3,5-Bis-trifluormethyl-aniso;Benzene, 1-methoxy-3,5-bis(trifluoromethyl)-;3,5-Bis(trifluoromethyl)anisole
CAS:349-60-0
MF:C9H6F6O
MW:244.13
EINECS:670-792-6
Product Categories:
Mol File:349-60-0.mol
3,5-Bis(trifluoromethyl)anisole Structure
3,5-Bis(trifluoromethyl)anisole Chemical Properties
Boiling point 158-160°C
density 1.352
refractive index 1.4075
Fp 158-160°C
storage temp. 2-8°C
AppearanceColorless to light yellow Liquid
BRN 2533238
CAS DataBase Reference349-60-0(CAS DataBase Reference)
Safety Information
Hazard Codes F
Risk Statements 10
Safety Statements 16
RIDADR 3271
Hazard Note Flammable
HazardClass 3
PackingGroup III
HS Code 2909309090
MSDS Information
ProviderLanguage
ALFA English
3,5-Bis(trifluoromethyl)anisole Usage And Synthesis
Synthesis
3,5-Bis(trifluoromethyl)bromobenzene

328-70-1

Sodium Methoxide

124-41-4

3,5-BIS(TRIFLUOROMETHYL)ANISOLE

349-60-0

The general procedure for the synthesis of 3,5-bis(trifluoromethyl)anisole from 3,5-bis(trifluoromethyl)bromobenzene and sodium methanol was as follows: 25 g of 1-bromo-3,5-bis(trifluoromethyl)benzene (85 mmol) was mixed with 366 mg of copper(I) bromide (CuBr, 3 mol%), 1.57 g of 18-crown-6 (7 mol%), and 92.3 g of sodium methanol in methanol ( 30% concentration, 21% precursor concentration) were mixed and heated to 105 °C. The reaction conversion was >97% as determined by GC (total reaction time 22 h). Subsequently, the reaction mixture was poured into 175 g of water and the pH was adjusted to 5-6 by dropwise addition of hydrochloric acid and then filtered through diatomaceous earth. The aqueous phase was extracted twice with 150 g of dichloromethane. The organic phases were combined and purified by vacuum fractional distillation to afford 16.5 g of 3,5-bis(trifluoromethyl)anisole (68 mmol, 79.4% yield) with a GC purity of >98.5%.

References[1] Patent: US2008/71084, 2008, A1. Location in patent: Page/Page column 4
Tag:3,5-Bis(trifluoromethyl)anisole(349-60-0) Related Product Information
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