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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180378Generated: October 30, 2026

Sodium hydride → Tert-butyl 4-{4-[[1-(methoxycarbonyl)-3-methylbutoxy](phenyl)methyl]benzoyl}piperazine-1-carboxylate

https://huagongshe.com/reaction/1180378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-bromo-4-methylpentanoateHCID 12957039—
ReactantTert-butyl 4-{4-[hydroxy(phenyl)methyl]benzoyl}piperazine-1-carboxylateHCID 69470269—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-{4-[[1-(methoxycarbonyl)-3-methylbutoxy](phenyl)methyl]benzoyl}piperazine-1-carboxylateHCID 69473035—

Reaction Steps

To a solution of tert-butyl 4-{4-[hydroxy(phenyl)methyl]benzoyl}piperazine-1-carboxylate from step 3 (1.5 g, 3.8 mmol) in DMF (20 mL) at 0° C. was added sodium hydride (0.16 g, 4.0 mmol) portionwise. The mixture was aged 15 minutes under a nitrogen atmosphere and methyl 2-bromo-4-methylpentanoate (0.65 mL, 4.0 mmol) was added dropwise. The reaction was allowed to warm to room temperature and was aged for 3 hours. The mixture was then partitioned between ethyl acetate and brine and the organic layer was dried and evaporated. The crude product was chromatographed on silica gel using 40% ethyl acetate in hexanes to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279478B2
Source datasetuspto-grants-2007_10
ORD IDord-da1fcdbca44645f18fa98c05880649b8
Source noteuspto-grants-2007_10