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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374735Generated: November 1, 2026

o-Toluenesulfonyl chloride → HCID 88196538, compound

https://huagongshe.com/reaction/374735

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 54296596HCID 54296596—
SolventDichloromethaneHCID 6344—
ProductHCID 88196538HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482650
Source datasetuspto-grants-1996_01
ORD IDord-6a32166e239548fd991804aab3bc2bc3
Source noteuspto-grants-1996_01