| Identification | More | [Name]
N-(2-Bromoethyl)phthalimide | [CAS]
574-98-1 | [Synonyms]
2-(2-BROMO-ETHYL)-ISOINDOLE-1,3-DIONE
AURORA KA-575
BETA-BROMOETHYLPHTHALIMIDE
LABOTEST-BB LT00439821
N-(2-BROMOETHYL)PHTALIMIDE
N-(2-BROMOETHYL)PHTHALIMIDE
N-(2-BROMOETHYLYL)-PHTALIMIDE
N-BROMOETHYLPHTHALIMIDE
SPECS AE-641/00791032
TIMTEC-BB SBB003129
1-Bromo-2-phthalimidoethane
1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-
2-(2-Bromoethyl)-1H-isoindole-1,3(2H)-dione
2-(2-bromoethyl)-1h-isoindole-3(2h)-dione
2-(2-Bromoethyl)phthalimide
2-(Bromoethyl)phthalimide
2-Phthalimidoethyl bromide
beta-Phthalimidoethyl bromide
b-Phthalimidoethyl bromide
-Bromoethylphthalimide | [EINECS(EC#)]
209-379-9 | [Molecular Formula]
C10H8BrNO2 | [MDL Number]
MFCD00005902 | [Molecular Weight]
254.08 | [MOL File]
574-98-1.mol |
| Safety Data | Back Directory | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29251995 |
| Hazard Information | Back Directory | [Chemical Properties]
white powder | [Uses]
N-(2-Bromoethyl)phthalimide is an intermediate used in organic synthesis. It can react with phenyl magnesium bromide to get 2-(2-bromo-ethyl)-3-hydroxy-3-phenyl-isoindolin-1-one. | [Synthesis Reference(s)]
Journal of the American Chemical Society, 71, p. 2425, 1949 DOI: 10.1021/ja01175a052
Organic Syntheses, Coll. Vol. 1, p. 119, 1941 | [Purification Methods]
The following is to be carried out in an efficient FUME HOOD. Dissolve the compound (180g) in CS2 (500 mL) by refluxing for 15minutes (to cause the separation of the most likely impurity, 1,2-diphthalimidoethane), filter and evaporate under reduced pressure. The product forms light tan crystals (m 78-80o). Recrystallise it from EtOH (charcoal) [the compound (50g) is dissolved in hot 75% EtOH (200mL), boiled for ca 10 minutes, carbon is added (5g, Norite), filter and cool to 0o], to give white crystals (40g) which can be recrystallised (m 80-81o); and further recrystallisation gives m 82-83o. [Salzberg & Supniewski Org Synth Coll Vol I 119 1932, Landini & Rolla Synthesis 389 1976, Beilstein 21/10 V 275.] |
|
|