Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Nitrilooxonium tetrafluoroborate | HCID 11137142 | — |
| Reactant | HCID 68006887 | HCID 68006887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67957780 | HCID 67957780 | — |
Reaction Steps
262 mg (0.89 mmol) of tert-butyl 1-[1-(4-chlorophenyl)propyl]cyclopropanecarboxylate were dissolved in 8 ml of dichloromethane, the mixture was cooled to 0° C. and 284 mg (2.14 mmol) of nitrosyl tetrafluoroborate were added a little at a time. The reaction solution was then stirred at a temperature between −10° C. and 0° C. for four hours. The reaction mixture was then added to water and extracted three times with dichloromethane. The combined organic phases were dried over magnesium sulphate and concentrated under reduced pressure. This gave 262 mg of the target product, which was used without further purification in the subsequent step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09018258B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-75c97c672d7149f285bf83d3a6434880 |
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| Source note | uspto-grants-2015_04 |
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