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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837839Generated: October 30, 2026

HCID 10712156, compound → HCID 11045622, compound

https://huagongshe.com/reaction/1837839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10712156HCID 10712156—
ReactantHCID 13214238HCID 13214238—
ProductHCID 11045622HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784305B2
Source datasetuspto-grants-2004_08
ORD IDord-54da5617482745b8b3c80696c4db1602
Source noteuspto-grants-2004_08