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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884176Generated: November 1, 2026

4-Chlorotoluene → HCID 10130194, compound

https://huagongshe.com/reaction/1884176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorotolueneHCID 7810—
ReactantPiperidineHCID 8082—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 10130194HCID 1013019460.5%

Reaction Steps

The general procedure from Example 1A was followed using 4-methyl-chlorobenzene (152 mg, 1.2 mmol) and piperidine (100 μl, 1.0 mmol) with Pd2(dba)3 (20 mg, 0.0218 mmol) and (Me3C)2PH(O) (14.5 mg, 0.0878 mmol) and NaOtBu (144 mg, 1.5 mmol) in 3.0 mL of toluene. After 12 h, the reaction mixture was chromatographed with 5% ethyl acetate/hexane to give 106 mg (δ1% yield) of N-(4-methylphenyl)piperidine. It was >95% pure by 1H NMR and GC/MS. 1H NMR (500 MHz, CDCl3): δ6.92 (d, J=8.4 Hz, 2H), 6.72 (d, J=8.5 Hz, 2H), 2.95 (t, J=5.5 Hz, 4H), 2.13 (s, 3H), 1.58 (m, 4H),1.43 (m, 2H) ppm. 13C NMR (125 MHz, CDCl3): δ150.3, 129.5, 128.6, 116.9, 51.2, 25.9, 24.3, 20.3 ppm. MS: Calculated for C12H17N(M+): 175.1. Found: 176.1 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762330B2
Source datasetuspto-grants-2004_07
ORD IDord-ccdfa3ebca2c41a9ad28c379450470de
Source noteuspto-grants-2004_07