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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2107137Generated: October 30, 2026

Tosylacetonitrile → HCID 23047706, compound

https://huagongshe.com/reaction/2107137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTosylacetonitrileHCID 79776—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 10753909HCID 10753909—
SolventBenzeneHCID 241—
ProductHCID 23047706HCID 23047706—

Reaction Steps

A mixture of 4.5 g (17.2 mmol) of 5-(4-chlorophenyl)pentyl bromide, 3.36 g (17.2 mmol) of (4-methylphenyl)sulfonylacetonitrile, 2.26 g (17.2 mmol) of 1,8-diazabicyclo(5,4,0)undec-7-ene and 30 ml of benzene is stirred at room temperature for 6 hours. Then the reaction mixture is washed with water; the organic phase is dried, and concentrated. The concentrate is chromatographed with a mixture of toluene and dioxane (10:1) on silica gel. Yield: 4.2 g (65% of theory) of the title compound, a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04933367
Source datasetuspto-grants-1990_06
ORD IDord-9074b1b64ab44c1fabdba6ccab24ca47
Source noteuspto-grants-1990_06