Ammonia → N-{[Dimethoxy(methyl)silyl]methyl}aniline

HRID 1176806Notes

Reaction equation

HRID 1176806 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl[CH2:9][Si:10]([CH3:15])([O:13][CH3:14])[O:11][CH3:12].N.[Cl-]>>[C:2]1([NH:1][CH2:9][Si:10]([O:13][CH3:14])([O:11][CH3:12])[CH3:15])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

5

Conditions

Temperature
30 °C

Procedure

In a 500 ml four-neck flask with reflux condenser, precision glass stirrer, thermometer and gas inlet tube, 298 g of dry aniline were heated to 130° C. and admixed with 124 g of (chloromethyl)methyl-dimethoxysilane with stirring within 60 min. When the addition had ended, ammonia was passed through the mixture with uniform temperature with stirring until no further reaction was observed (approx. 60 min). Thereafter, excess aniline was removed under reduced pressure, and the suspension was cooled to 30° C. and then admixed with 150 ml of isohexane. Subsequently, the white precipitate formed was filtered through a suction filter and washed with 2×80 ml of isohexane. Filtrate and wash solutions were combined and freed from the solvent under reduced pressure. The subsequent fractional distillation gave 160 g (95% yield) of (N-phenylaminomethyl)dimethoxy(methyl)silane with a chloride content of <20 ppm.

Workup

  1. temperatureIn a 500 ml four-neck flask with reflux condenser, precision glass stirrer
  2. additionWhen the addition
  3. stirringwith stirring until no further reaction
  4. custom(approx. 60 min)
  5. customThereafter, excess aniline was removed under reduced pressure
  6. customSubsequently, the white precipitate formed
  7. filtrationwas filtered through a suction
  8. filtrationfilter
  9. washwashed with 2×80 ml of isohexane
  10. washFiltrate and wash solutions
  11. distillationThe subsequent fractional distillation

Sources & evidence

ORD record
ord-2c7c60276a9f499383f2fc81e2867b8c
Source dataset
uspto-grants-2010_11
Patent number
US07842831B2

Reaction notes

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