Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Silane, (bromomethyl)chlorodimethyl- | HCID 85476 | — |
| Reactant | HCID 22717044 | HCID 22717044 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22717055 | HCID 22717055 | — |
Reaction Steps
A solution of tert-butyl 4-[3-bromo-5-(trifluoromethyl)-phenyl]-1-piperazine carboxylate (75 g, 183 mmoles) in diethyl ether, previously dried on molecular sieves, (1000 ml) was cooled to −65° C. and a 1.7M solution of tert-butyl lithium (215,6 ml, 366 mmoles) was added. After 30 minutes stirring bromomethyl-dimethyl-chlorosilane (49.9 ml, 366 mmoles) was added dropwise. After 2 hours stirring at −65° C., the reaction mixture was left at room temperature overnight. Water (600 ml) was added and the organic layer was washed with water, dried on MgSO4, filtered and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740712B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-24cfd2dd5a5441608ced478c2ce88a30 |
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| Source note | uspto-grants-2004_05 |
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