HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Toluenesulfonyl chloride → HCID 88196538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Toluenesulfonyl chloride | HCID 8623 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54296596 | HCID 54296596 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 88196538 | HCID 88196538 | — |
Reaction Steps
This hexanol (1.2 g, 2.45 Moles)was combined with toluene sulfonyl chloride (0.5 g, 2.58 mmoles), N,N-diisopropylethyl amine (0.85 mL, 4.9 mmoles), and N,N-dimethylaminopyridine (12 mg, 0.98 mmole) in dichloromethane (10 mL). After stirring for 10 hours at room temperature, the desired product, 1-toluenesulfonyl-6,6-difluoro-6-(perfluoro-2-butoxyethoxy)hexane, was isolated by column chromatography (and its structure confirmed by infrared spectroscopy).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05482650 |
| Source dataset | uspto-grants-1996_01 |
| ORD ID | ord-6a32166e239548fd991804aab3bc2bc3 |
| Source note | uspto-grants-1996_01 |