Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Benzyl 2,2,2-trichloroacetimidate | HCID 144968 | — |
| Reactant | 62957-46-4 | HCID 11041090 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59594958 | HCID 59594958 | 52% |
Reaction Steps
To a solution of 1-methyl-4-bromo-1-butanol (9.0 g, 0.05384 mol) and benzyl 2,2,2-trichloroacetimidate (16.3 g,) in a mixture of anhydrous cyclohexane (100 ml) and anhydrous dichloromethane (50 ml) cooled to 0° C., trifluoromethanesulfonic acid (1.0 ml) was added, and the mixture was stirred overnight at room temperature under argon. The mixture was filtered, washed with a saturated solution of NaHCO3 (250 ml) and deionized water (250 ml), and dried with anhydrous Na2SO4. The solvents were removed by distillation under reduced pressure. The crude product (9.2 g) was subjected to vacuum distillation, giving 7.2 g of colorless viscous liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492488B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ef519b9184644717b34fc46ef329cb77 |
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| Source note | uspto-grants-2013_07 |
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