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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716571Generated: November 1, 2026

Sodium hydride → HCID 68505590, compound

https://huagongshe.com/reaction/1716571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantHCID 68514185HCID 68514185—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68505590HCID 68505590—

Reaction Steps

A stirring solution of racemic trans-3-hydroxy-4-[2,5-dimethylbenzimidazol-1yl]-N-Boc-piperidine (950 mg; 2.75 mmol) in THF (30 mL) under Ar cooled to 0° C. NaH (60% oil dispersion; 132 mg; 3.3 mmol) was added and the mixture was stirred for 15 min followed by addition of tert-butyl bromoacetate (516 μL; 3.5 mmol). The reaction mixture was warmed to rt and allowed to stir for 14 hours after which it was poured into satd NH4Cl and extracted three times with ethyl acetate. The combined organic layers were washed with brine and dried over MgSO4. Filtration followed by removal of volatiles under reduced pressure yielded crude product. Racemic 3-tert-butoxycarbonylmethoxy-4-(2,5-dimethyl-benzoimidazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester was isolated as an oil by flash chromatography (470 mg; 37%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803816B2
Source datasetuspto-grants-2010_09
ORD IDord-d746fe0ea29f4a31957d271e4fff0ced
Source noteuspto-grants-2010_09