HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10712156, compound → HCID 11045622, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10712156 | HCID 10712156 | — |
| Reactant | HCID 13214238 | HCID 13214238 | — |
| Product | HCID 11045622 | HCID 11045622 | — |
Reaction Steps
Preparation and handling of organometallic compounds were carried out in the absence of air and moisture under argon (Schlenk technique or glove box). All solvents required were purged with argon and dried over molecular sieves before use. 1,2-Bistrifluoromethylsulfonyloxyethane was synthesized as described by Lindner, Ekkehard; Au, Guenter von; Eberle, Hans-Juergen; Chem.Ber.; 114; 2; 1981; 810-813. The preparations of 1,3-bistrifluoromethylsulfonyloxypropane and 1,2-bistrifluoromethylsulfonyloxycyclohexane were carried out analogously. The indenes used were prepared as described in WO 9840331.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06784305B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-54da5617482745b8b3c80696c4db1602 |
| Source note | uspto-grants-2004_08 |