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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596839Generated: October 30, 2026

4-Chlorotoluene → HCID 10130194, compound

https://huagongshe.com/reaction/1596839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorotolueneHCID 7810—
ReactantPiperidineHCID 8082—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
ProductHCID 10130194HCID 1013019461%

Reaction Steps

The general procedure from Example 1 was followed using 4-methylchlorobenzene (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 (61% yield) of N-(4-methylphenyl)piperidine. It was >95% pure by 1H NMR and GC/MS. 1H NMR (500 MHz, CDCl3): δ 6.92 (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): δ 150.3, 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 numberUS06291722B1
Source datasetuspto-grants-2001_09
ORD IDord-f59e60bfb0cd4cda8b94caa711237af3
Source noteuspto-grants-2001_09