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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376647Generated: October 31, 2026

Sodium hydride → tert-Butyl 4-(3-chlorophenyl)-4-cyanopiperidine-1-carboxylate

https://huagongshe.com/reaction/2376647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactantm-ChlorophenylacetonitrileHCID 73722—
ReactantN-BOC-N,N-Bis(2-chloroethyl)amineHCID 11230235—
SolventDimethyl SulfoxideHCID 679—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-(3-chlorophenyl)-4-cyanopiperidine-1-carboxylateHCID 49760302—

Reaction Steps

A suspension of 15.8 g of sodium hydride of a concentration of 60% in oil in 400 ml of DMSO is admixed dropwise at AT under an inert atmosphere with a solution of 30 g of 3-chlorophenylacetonitrile in 200 ml of THF and then with a solution of 45.5 g of tert-butyl bis(2-chloroethyl)carbamate in 200 ml of DMSO and is heated at 60° C. overnight. The reaction mixture is poured into an ice/water mixture and extracted with ether, the organic phase is washed with water and dried over Na2SO4 and the solvent is evaporated under vacuum. The residue is chromatographed on silica gel, eluting with DCM. This gives 33 g of the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468368B2
Source datasetuspto-grants-2008_12
ORD IDord-a29898ac28494aeead4771172a138aa1
Source noteuspto-grants-2008_12