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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426374Generated: October 30, 2026

1-Iodopropane → HCID 11712446, compound

https://huagongshe.com/reaction/426374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 11618716HCID 11618716—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 11712446HCID 1171244661%

Reaction Conditions

Temperature120 °C

Reaction Steps

A 20 mL vial was charged with 5d (763 mg, 1.79 mmol), and NMP (10 mL). The vial was capped with a septum and placed in an oil bath heated to 120° C. DBU (267 μL, 1.79 mmol) was added, and the mixture was stirred for 2 min. Then iodopropane (175 μL, 1.79 mmol) was added and the mixture was stirred for 20 min. A second dose of DBU (267 μL, 1.79 mmol), followed by iodopropane (175 μL, 1.79 mmol), was added, and 20 min later, a third identical round of DBU and iodopropane was again added. After the third round of reagents was added and the mixture was stirred for 20 min, the reaction mixture was removed from heat and added to ethyl acetate. The solution was washed three times with water, then washed with brine, dried over Na2SO4, filtered, and concentrated to dryness. The residue was chromatographed (silica, CHCl3), yielding a colorless solid (506 mg, 61%): mp 242-243° C.; 1H NMR (d6-acetone) δ 0.89 (t, J=7.2 Hz, 3H), 1.17-1.19 (m, 21H), 1.86-1.96 (m, 2H), 4.53 (t, J=7.6 Hz, 2H), 7.75 (d, J=8.0 Hz, 2H), 7.91 (d, J=8.0 Hz, 2H), 8.36 (s, 1H), 8.50 (s, 1H); 13C NMR (d6-acetone) δ 10.5, 11.3, 18.4, 23.2, 47.1, 93.1, 106.6, 108.1, 108.3, 116.8, 116.9, 118.3, 125.8, 126.3, 129.6, 129.9, 132.5, 138.5, 145.4, 158.4; Anal. Calcd for C29H34N4Si: C, 74.63; H, 7.34; N, 12.01. Found: C, 74.75; H, 7.32; N, 12.01.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106393B2
Source datasetuspto-grants-2012_01
ORD IDord-94dcd1a033b74d3d9e811a896fdbe99a
Source noteuspto-grants-2012_01