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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093889Generated: November 1, 2026

Dipropylamine → HCID 9920908, compound

https://huagongshe.com/reaction/1093889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantCesium carbonateHCID 10796—
ReactantPotassium BromideHCID 253877—
Reactant3-Vinyl-cyclohex-2-enoneHCID 11768562—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 9920908HCID 9920908—

Reaction Steps

3-Vinyl-cyclohex-2-enone (0.75 g, 6.1 mmol) (prepared according to Nasarow's method) was dissolved in acetonitril (1 mL) and dipropylamine (1.5 g, 16 mmol) was added followed by Cs2CO3 (50 mg). After stirring the mixture at rt for 3 h it was diluted with diethylether (100 mL), filtered and evaporated to dryness. The residue was destined in vacuo (175° C., 0.01 mm Hg) to give a slightly yellow oil which was converted to the hydrochloride salt. Recrystallization from isopropyl ether/isopropyl alcohol yielded: 1.2 g, 4.6 mmol (75%), mp 95-97° C. IR (KBr) 2962, 2613, 1667; 1H-NMR (CDCl3) δ 5.84 (d, 1H), 2.65 (m, 2H), 2.27-2.60 (m, 9H), 1.99 (m, 2H), 1.39-1.51 (m, 5H), 0.86 (t, 6H) ppm; 13C-NMR (CDCl3) δ 198.2, 163.5, 124.9, 54.2, 50.1, 35.7, 33.7, 28.4, 21.2, 18.5, 10.4 ppm; MS (EI) m/z 223 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE043244E1
Source datasetuspto-grants-2012_03
ORD IDord-32e439c18a7b46d8af61d3e3d313d0a2
Source noteuspto-grants-2012_03