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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536221Generated: October 26, 2026

Triethylamine → Triethylammonium bromide

https://huagongshe.com/reaction/536221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyanogen BromideHCID 10476—
Reactant2-(4,5-dihydro-1H-imidazol-2-yl)-6-methoxyanilineHCID 58377357—
SolventDichloromethaneHCID 6344—
ProductTriethylammonium bromideHCID 2734074296.1%
ProductHCID 178488375HCID 178488375—

Reaction Conditions

Temperature10 °C

Reaction Steps

2-(4,5-Dihydro-1H-imidazol-2-yl)-6-methoxyaniline (Step 3, 22.0 g, 115 mmol) and Et3N (48.1 mL, 345 mmol) were dissolved in CH2Cl2 (200 mL), cooled to 10° C. in an ice bath and cyanogen bromide (24.4 g, 230 mmol) was added portionwise. A slight exotherm was noted, and the reaction was stirred overnight. The reaction was concentrated under reduced pressure, then treated with EtOAc (150 mL) and concentrated under reduced pressure again. Finally, the residue was treated with Heptane and concentrated under reduced pressure to give the title compound as a mixture with Et3N.HBr (62 g, 99%): HPLC MS RT=1.08 min, MH+=217.1; 1H NMR (DMSO-d6+2 drops TFA-d) δ: 3.85 (3H, s), 4.09-4.16 (2H, m), 4.31-4.38 (2H, m), 7.23 (1H, t), 7.31 (1H, d), 7.57 (1H, dd).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859572B2
Source datasetuspto-grants-2014_10
ORD IDord-cbf1799c49494e7eaaac2cf948a53bb4
Source noteuspto-grants-2014_10