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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242603Generated: November 1, 2026

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

https://huagongshe.com/reaction/2242603

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 numberUS07671235B2
Source datasetuspto-grants-2010_03
ORD IDord-c122a5c2cc6b4de4ada5246f4153650e
Source noteuspto-grants-2010_03