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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404467Generated: October 31, 2026

Phenol → HCID 178480513, compound

https://huagongshe.com/reaction/2404467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHCID 178480516HCID 178480516—
SolventChloroformHCID 6212—
ProductHCID 178480513HCID 178480513—

Reaction Steps

To a solution of (2-{3-[(5-fluoro-1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethyl)carbamic acid tert-butyl ester (example 437C, 386 mg) in chloroform (10 mL) are added phenol (750 mg) and chlorotrimethylsilane (814 mg). The mixture is heated at reflux for 2 h. The solvent and volatiles are removed under reduced pressure. The residue is basified by adding a solution of 1N sodium hydroxide. The aqueous phase is extracted by ethyl acetate. The organic phase is washed by water, then dried over magnesium sulfate and concentrated. The residue is purified by chromatography on silica gel (gradient dichloromethane/methanol/ammonia from 100/0/0 to 90/10/1) to give 2-{3-[(5-fluoro-1H-benzimidazol-2-yl)(1-methylpiperidin-4-yloxy)methyl]phenylsulfanyl}ethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802664B2
Source datasetuspto-grants-2014_08
ORD IDord-f60e01f6b9d04e979caabeb017deaf97
Source noteuspto-grants-2014_08