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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339178Generated: October 28, 2026

Ethanol → 6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile

https://huagongshe.com/reaction/339178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant6-Benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrileHCID 59021756—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
Product6-Benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrileHCID 5902174990.1%

Reaction Steps

6-Benzenesulfonyl-3,4-dihydro-naphthalene-1-carbonitrile (5.1 g, 17.2 mmol), 70 mL EtOH, and 50 mL acetic acid were placed in a Parr vessel, and 1.0 g of 10% Palladium on carbon (Fluka Chemica Co.) was added. The reaction mixture was shaken for 15 hours under 55 psi hydrogen. The Parr vessel was purged with nitrogen and the reaction mixture was filtered. The filtrate was added to 500 mL water, and the aqueous mixture was extracted twice with 200 mL of EtOAc. The combined organic layers were dried (MgSO4) and evaporated to yield 4.6 g (15.5 mmol, 90%) of 6-benzenesulfonyl-1,2,3,4-tetrahydro-naphthalene-1-carbonitrile as an oil. MS: 298 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889906B2
Source datasetuspto-grants-2014_11
ORD IDord-2de491ac4047468eb5ba0f8a507723f7
Source noteuspto-grants-2014_11