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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897382Generated: October 31, 2026

1-Bromooctane → HCID 86646635, compound

https://huagongshe.com/reaction/1897382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctaneHCID 8140—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178488803HCID 178488803—
SolventDimethylformamideHCID 6228—
ProductHCID 86646635HCID 8664663531.8%

Reaction Conditions

Temperature120 °C

Reaction Steps

4-methoxyacridin-9-ol (2.0 g, 8.88 mmol), 1-bromooctane (2.17 g, 11.24 mmol), and potassium carbonate (7.91 g, 57.2 mmol) was mixed in N,N-dimethylformamide and heated at 120° C. for 8 h and the potassium carbonate was filtered off. The reaction mixture was quenched with water and extracted two times with ether and the combined organic phases was then washed once with 1M HCl, two times with water, and evaporated to obtain a yellow solid. The solid was recrystallised in methanol to give 4-methoxy-9-(octyloxy)acridine (0.95 g, 2.82 mmol) as yellow crystals. 1H-NMR (CDCl3, 5): 0.881 (t, 3H), 1.2-1.4 (m, 10H), 1.924 (m, 2H), 3.985 (s, 3H), 4.507 (t, 2H), 7.2-7.3 (m, 3H), 7.621 (d, 1H), 7.707 (m, 1H), 8.181 (m, 1H), 8.498 (m, 1H) MS MALDI-TOF (m/z): 337.146

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08519037B2
Source datasetuspto-grants-2013_08
ORD IDord-98a869e0e18248a2b82867833eeb268e
Source noteuspto-grants-2013_08