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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381732Generated: November 1, 2026

Dimethylformamide → 10-Bromoanthracene-9-carbaldehyde

https://huagongshe.com/reaction/1381732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant9,10-DibromoanthraceneHCID 68226—
ReactantButyllithiumHCID 178418339—
Product10-Bromoanthracene-9-carbaldehydeHCID 600743—

Reaction Steps

This material was made from 9,10 dibromoanthracene (Eastman, 20 g, 60 mmol) modifying the procedure of R. Kuhn and H. Fischer, Chem. Ber. 94 3060 (1961). In this procedure, the reaction mixture was cooled to -78° before the nBuLi was added. The resulting mixture was warmed to RT over 1 H and then refluxed until the crystalline starting material disappeared. The mixture was then cooled to -78° again before the DMF was added (in one portion). The flask was warmed to RT and then quenched with 1M HBr (200 mL). The two-phase system was then extracted with CH2Cl2 (3×500 mL). The extracts combined, dried (MgSO4), filtered, and the solvent removed to give the crude material. This was purified by preparative HPLC using PhCH3 as the eluting solvent. After the solvent was removed 13.06 g (76%) of 10-bromo-9-anthracenecarbaldehyde mp 215°-216.5°, lit. mp 218°, P. Kuhn and H. Fischer, Chem. Ber. 94 3060 (1961)), (C, H, Br) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803226
Source datasetuspto-grants-1989_02
ORD IDord-7c8af183297f45958be17f26311fda48
Source noteuspto-grants-1989_02