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CAS RN: 33797-51-2 | Product Number: D1646

N,N-Dimethylmethyleneammonium Iodide


Purity: >97.0%(T)
Synonyms:
  • Eschenmoser's Salt
  • N,N-Dimethylmethyleneiminium Iodide
Documents:
5G
£38.00
1   ≥20 
25G
£116.00
4   17  

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Product Number D1646
Purity / Analysis Method >97.0%(T)
Molecular Formula / Molecular Weight C__3H__8IN = 185.01  
Physical State (20 deg.C) Solid
Storage Temperature 0-10°C
Store Under Inert Gas Store under inert gas
Condition to Avoid Light Sensitive,Moisture Sensitive,Heat Sensitive
CAS RN 33797-51-2
Reaxys Registry Number 3594966
PubChem Substance ID 87568123
SDBS (AIST Spectral DB) 19772
Merck Index (14) 3251
MDL Number

MFCD00011810

Specifications
Appearance White to Gray to Brown powder to crystal
Purity( Potassium iodate Method) min. 97.0 %
Properties (reference)
GHS
Pictogram Pictogram
Signal Word Warning
Hazard Statements H315 : Causes skin irritation.
H319 : Causes serious eye irritation.
Precautionary Statements P264 : Wash skin thoroughly after handling.
P280 : Wear protective gloves/ eye protection/ face protection.
P302 + P352 : IF ON SKIN: Wash with plenty of water.
P337 + P313 : If eye irritation persists: Get medical advice/ attention.
P362 + P364 : Take off contaminated clothing and wash it before reuse.
P332 + P313 : If skin irritation occurs: Get medical advice/ attention.
Related Laws:
EC Number 251-680-2
Transport Information:
HS Number 2923900090
Application
Bromination

Typical Procedure:
To a cold (-20 °C) solution of diisopropylamine (50 mg, 0.492 mmol) in THF (630 µL) is added the solution of n-butyllithium in hexane (294 µL of the 1.67 M solution, 0.491 mmol). The solution is stirred for 15 min at that temperature, then cooled to -78 ℃ and the solution of 1 (91.3 mg, 0.447 mmol) in THF (400 µL) is added. HMPA (319 mg, 1.78 mmol) is added to the solution of the lithium enolate, and the resulting solution is transferred via cannula to a cold (-78 °C) suspension of the Eschenmoser's salt (200 mg, 1.08 mmol) in THF (1 mL). The reaction mixture is allowed to reach rt with stirring, when the yellow suspension turned into solution. The reaction is quenched with saturated aqueous NaHCO3 (10 mL) and the product is extracted with ethyl acetate (4 x 25 mL). The organic extract is washed with brine, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. The crude residue (430 mg) is dissolved in diethyl ether (3 mL), methyl iodide (1 mL, 16.28 mmol) is added and the reaction mixture is stirred at rt for 2 hours. The solution of NaOAc (1.2 g) in water (7 mL) is added and the reaction mixture is vigorously stirred for 1 hour. The mixture is diluted with hexane (80 mL) and water (10 mL), the phases are separated and the aqueous phase is extracted with hexane (2 x 10 mL). The combined extract is thoroughly washed with water, dried over anhydrous MgSO4, filtered and concentrated under reduced pressure. Purification of the crude organic residue (107 mg) by column chromatography (gradient elution with hexane : diethyl ether = 95 : 5 → 9 : 1) affords 2 (28 mg, Y. 53%).

References


PubMed Literature


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