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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266981Generated: November 3, 2026

Chlorobenzene → HCID 13011971, compound

https://huagongshe.com/reaction/2266981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
Reactant223394-90-9HCID 10953873—
ReactantSodium t-butoxideHCID 23676156—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13011971HCID 1301197191%

Reaction Conditions

Temperature80 °C

Reaction Steps

Following general procedure F, a mixture of chlorobenzene (51 μL, 0.5 mmol), N1-phenylbutane-1,4-diamine (98 mg, 0.6 mmol), NaOt-Bu (97 mg, 1.0 mmol), 10 (4 mg, 1 mol %), 1 (2.5 mg, 1 mol %), and dioxane (0.5 mL) was heated to 80° C. for 2 h. The crude product was purified via the Biotage SP4 (silica-packed 50 g snap; 0-75% EtOAc/hexanes) to provide the title compound as a clear oil (108 mg, 91%). 1H NMR (300 MHz, CDCl3) δ: 7.28 (t, J=7.0 Hz, 4H), 6.80 (t, J=7.0 Hz, 2H), 6.68 (d, J=7.0 Hz, 4H), 3.68 (s, 2H), 3.22 (m, 4H), 1.78 (m, 4H) ppm. 13C NMR (75 MHz, CDCl3) δ: 148.6, 129.6, 117.6, 113.1, 44.0, 27.4 ppm. IR (neat, cm−1): 3407, 3050, 2934, 2861, 1603, 1507, 1477, 1321, 1257, 1179, 749, 693. Anal. Calcd. for C16H20N2: C, 79.96; H, 8.39. Found: C, 80.20; H, 8.48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858784B2
Source datasetuspto-grants-2010_12
ORD IDord-221caf56bc02464c9a375da3dd2cf5bc
Source noteuspto-grants-2010_12