Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | 1,3-Bis(iodomethyl)-1,1,3,3-tetramethyldisiloxane | HCID 256681 | — |
| Solvent | Water | HCID 962 | — |
| Product | 72821-03-5 | HCID 20333929 | — |
Reaction Steps
An amount of 33.6 g. (0.315 mole) of benzylamine is added over a period of approximately 5 minutes to 41.4 g. (0.1 mole) of 1,3-bis-iodomethyl-1,1,3,3-tetramethyl-disiloxane with stirring in a bath at room temperature. Stirring is continued at room temperature for one hour. (A slurry resulted). Addition of 50 ml. of acetonitrile gives a clear solution which is then heated to reflux for 2 hours. The cooled solution is distributed between approximately 0.5 l. of pentane and 1.5 l. of water. The aqueous layer is then extracted with one more approximately 200 ml. portion of pentane, and the combined organic layer is washed twice with approximately 300 ml. of water, dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to provide a clear yellow mobile liquid. This product is then vacuum distilled to give 4-benzyl-2,2,6,6-tetramethyl-1-oxa-4-aza-2,6-disilacyclohexane; b.p. 134° to 135° C., at 13 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04208408 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-1590b6c79e544e76948a513e2650e065 |
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| Source note | uspto-grants-1980_06 |
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