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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309619Generated: October 25, 2026

Sodium hydride → ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]oxy]-1-piperidinecarboxylate

https://huagongshe.com/reaction/2309619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantEthyl 4-hydroxypiperidine-1-carboxylateHCID 96394—
Reactant1-(4-Fluorobenzyl)-2-chlorobenzimidazoleHCID 3020241—
SolventDimethylformamideHCID 6228—
Productethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]oxy]-1-piperidinecarboxylateHCID 1401330431.5%

Reaction Steps

To a stirred mixture of 3.5 parts of ethyl 4-hydroxy-1-piperidinecarboxylate and 135 parts of N,N-dimethylformamide was added 1 part of a sodium hydride dispersion 50% and stirring was continued for 2 hours at room temperature. After the addition of 5.2 parts of 2-chloro-1-[(4-fluorophenyl)methyl]-1H-benzimidazole, the whole was further stirred overnight at room temperature. The reaction mixture was poured into ice water and the product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from 2,2'-oxybispropane, yielding 2.5 parts (31.5%) of ethyl 4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]oxy]-1-piperidinecarboxylate; mp. 94.0° C. (26).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695575
Source datasetuspto-grants-1987_09
ORD IDord-02960a98118b4ed88931ea42f361b320
Source noteuspto-grants-1987_09