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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841547Generated: October 30, 2026

Hydrogen Bromide → HCID 22482479, compound

https://huagongshe.com/reaction/841547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHCID 492672HCID 492672—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
SolventAcetic AcidHCID 176—
ProductHCID 22482479HCID 2248247986%

Reaction Steps

To 1-(2,6-difluorobenzyl)-2-(2,6-difluorophenyl)-4-methoxylbenzimidazole (Example 46) (0.30 g, 0.78 mmol) and hexadecyltrimethylammonium bromide (0.30 g) dissolved in acetic acid (9.0 mL) was added HBr (1.0 mL). After refluxing for 7 h, the reaction was concentrated. The residue was then diluted with EtOAc, and washed with NaHCO3 (sat. aq) and NaCl (sat. aq). The combined washing were dried (Na2SO4), filtered, and concentrated. The crude product was purified by flash chromatography eluting with 2% methanol/CH2Cl2 and recrystallization from diethylether, yielding 1-(2,6-Difluorobenzyl)-2-(2,6-difluorophenyl)-4-hydroxylbenzimidazole (0.25 g, 0.67 mmol, 86% yield). M.p. 257-259° C. 1H NMR (200 MHz, CD2Cl2): δ7.57 (m, 1H, H4′), 7.25 (m, 1H, H4″), 7.17 (dd, J=7.9, 8.3 Hz, 1H, H6), 7.12 (m, 2H, H3′,5′), 6.99 (d, J=8.3 Hz, 1H, H7), 6.82 (m, 2H, H3″,5″), 6.73 (dd, J=7.9, 1.0 Hz, H5), 5.35 (s, 2H, CH2PhF2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369235B1
Source datasetuspto-grants-2002_04
ORD IDord-d89e0215c9ee460180c2e8e11e79c0d3
Source noteuspto-grants-2002_04