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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698580Generated: November 1, 2026

Diethyl Ether → 3-{4-Chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-1-methyl-1H-benzimidazol-7-yl}-2,2,4,4-tetramethylpentan-3-ol

https://huagongshe.com/reaction/1698580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPentaneHCID 8003—
ReactantMethyl 4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-1-methyl-1H-benzimidazole-7-carboxylateHCID 67273388—
ReactantHCID 178418306HCID 178418306—
SolventWaterHCID 962—
Product3-{4-Chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-1-methyl-1H-benzimidazol-7-yl}-2,2,4,4-tetramethylpentan-3-olHCID 580123125%

Reaction Steps

A n-pentane solution of tert-butyl lithium (1.46 M, 0.5 ml) was added to a solution of methyl 4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-1-methyl-1H-benzimidazole-7-carboxylate (100 mg, 0.23 mmol) in diethyl ether (5 ml) at −78° C. and stirred for 1 h. The reaction mixture was diluted with water (5 mL), stirred at room temperature for 0.5 h and extracted with ethyl acetate. The organics was dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was purified by preparative HPLC. The resultant was neutralized with aqueous sodium hydrogen carbonate and extracted with ethyl acetate. The organics were dried over magnesium sulfate, filtered, and concentrated in vacuo to give 5 mg (0.010 mmol, 5%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163935B2
Source datasetuspto-grants-2012_04
ORD IDord-037c2eac36724987856f4c60928d8f71
Source noteuspto-grants-2012_04