Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | HCID 86758097 | HCID 86758097 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 9855190 | HCID 9855190 | — |
Reaction Steps
Potassium bis(tris(pentafluorophenyl)borane)cyanide (827.5 mg, 0.7598 mmol) and chlorotriphenylmethane (211.8 mg, 0.7597 mmol) were placed in a 50 mL flask. The stirred solids were taken up in 10 mL of dichloromethane, added via syringe under argon counter-flow. An immediate reaction gave a deep yellow solution and a colorless solid. The solid was removed by filtration and washed (four times 4 mL) until all color was gone. The filtrate was reduced under vacuum to 4 mL, cooled to −78° C. and diluted with 10 mL of hexanes. The resulting suspension of brown oil was allowed to warm and stir. The oil solidified and then digested to a canary-yellow solid after stirring for 30 minutes. The yellow solid was isolated by filtration and dried under high vacuum. Yield, 935.3 mg, 95.20 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06395671B2 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-e7f1cab81c7442a8a6c1fbc33d788b0c |
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| Source note | uspto-grants-2002_05 |
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