ChemicalBook--->CAS DataBase List--->343-93-1

343-93-1

343-93-1 Structure

343-93-1 Structure
IdentificationMore
[Name]

6-FLUOROGRAMINE
[CAS]

343-93-1
[Synonyms]

6-FLUOROGRAMINE
6-FLUOROFLAVONE
6-Fluorogramine 97%
3-(DIMETHYLAMINOMETHYL)-6-FLUOROINDOLE
6-FLUORO-3-[DIMETHYLAMINOMETHYL]-INDOLE
3-(Dimethylaminomethyl)-6-fluoro-1H-indole
[(6-fluoro-1H-indol-3-yl)methyl]dimethylamine
1H-Indole-3-methanamine, 6-fluoro-N,N-dimethyl-
(6-Fluoroindole-3-ylmethyl)dimethylamine (6-Fluorogramine)
[Molecular Formula]

C11H13FN2
[MDL Number]

MFCD00056918
[Molecular Weight]

192.23
[MOL File]

343-93-1.mol
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

343-93-1(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[Hazard Codes ]

Xi
[WGK Germany ]

3
[Hazard Note ]

Irritant
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

6-FLUOROGRAMINE(343-93-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

343-93-1(sigmaaldrich)
Hazard InformationBack Directory
[Synthesis]

6-Fluoroindole

399-51-9

Formaldehyde

50-00-0

Dimethylamine

124-40-3

6-FLUOROGRAMINE

343-93-1

An aqueous solution of about 40% dimethylamine (35.68 kg, 1.0 eq.) was added to a 250 L reaction vessel under nitrogen protection and the mixture was cooled to about 4.5 °C. Glacial acetic acid (43.4 kg, 2.5 eq.) was slowly added dropwise over a period of 140 minutes while the reaction temperature was controlled to not exceed 15°C. After the dropwise addition was completed, stirring was continued for 20 minutes at about 3°C. Subsequently, 37% formaldehyde aqueous solution (25.9 kg, 1.1 eq.) was slowly added over about 20 minutes, keeping the reaction temperature between 0°C and 10°C. Upon addition of 6-fluoroindole (39.2 kg), the reaction was exothermic raising the temperature to about 40°C and subsequently cooled to about 20°C. The reaction solution was slowly transferred to a 650 L reactor filled with 3M NaOH aqueous solution, taking about 40 minutes. The resulting suspension was stirred at 5°C to 20°C for 40 minutes, the product was collected by filtration, washed with deionized water (120 kg) and dried at 50°C to afford 1-(6-fluoro-1H-indol-3-yl)-N,N-dimethylmethylamine (45.4 kg, 85% yield).

[References]

[1] Patent: US2011/152539, 2011, A1. Location in patent: Page/Page column 4
[2] Patent: US2016/168089, 2016, A1. Location in patent: Page/Page column 0081; 0082
[3] Chemical Communications, 2016, vol. 52, # 34, p. 5868 - 5871
[4] Journal of Organic Chemistry, 2018, vol. 83, # 17, p. 9902 - 9913
[5] Patent: WO2010/36362, 2010, A1. Location in patent: Page/Page column 44
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