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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266982Generated: October 31, 2026

Chlorobenzene → HCID 57495494, compound

https://huagongshe.com/reaction/2266982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
Reactant4-(Aminomethyl)piperidineHCID 23527—
ReactantSodium t-butoxideHCID 23676156—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57495494HCID 5749549484%

Reaction Conditions

Temperature80 °C

Reaction Steps

Following general procedure F, a mixture of chlorobenzene (102 μL, 1.0 mmol), 4-(aminomethyl)piperidine (137 mg, 1.2 mmol), NaOt-Bu (192 mg, 2.0 mmol), 10 (8 mg, 1 mol %), 1 (5 mg, 1 mol %), and dioxane (1 mL) was heated to 80° C. for 15 h. The crude product was purified via the Biotage SP4 (silica-packed 50 g snap; 7-9% MeOH/CH2Cl2) to provide the title compound as a white solid (159 mg, 84%), mp 60-61° C. 1H NMR (300 MHz, DMSO) δ: 7.02 (t, J=7.5 Hz, 2H), 6.52 (d, J=8.0 Hz, 2H), 6.46 (t, J=8.0 Hz, 1H), 5.58 (s, 1H), 3.11 (s, 1H), 2.92 (d, J=11.5 Hz, 2H), 2.82 (t, J=6.0 Hz, 2H), 2.41 (t, J=10 Hz, 2H), 1.64 (m, 3H), 1.02 (m 2H) ppm. 13C NMR (75 MHz, DMSO) δ: 149.8, 129.5, 115.8, 112.5, 50.0, 46.5, 36.2, 31.7 ppm. IR (neat, cm−1): 3326, 2919, 1602, 1509, 1427, 1325, 1263, 749, 694.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858784B2
Source datasetuspto-grants-2010_12
ORD IDord-315187e0d5df4d11985bcefdbeeb38a1
Source noteuspto-grants-2010_12