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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272517Generated: November 4, 2026

Dimethyl Sulfate → HCID 18457671, compound

https://huagongshe.com/reaction/1272517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTert-butyl 4-piperidin-1-ylpiperidine-1-carboxylateHCID 14571191—
ReactantCID 53628100HCID 178418400—
SolventDiethyl EtherHCID 3283—
ProductHCID 18457671HCID 18457671—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1′-tert-Butoxycarbonyl-[1,4′]-Bipiperidine 1 (5.1 g, 19.0 mmol), TMEDA (19 ml) in dry Et2O (40 ml) at −78° C. is slowly added a solution of sec-butyllithium (19.0 ml, 24.7 mmol, 1.3 M in cyclohexanes) over a period of 30 min. The mixture is stirred at −78° C. for 3 hr, and then is treated with a solution of Dimethylsulfate (3.6 g, 28.5 mmol) in Et2O (5 ml). The cooling bath is removed and the reaction mixture is stirred at ambient temperature for 16 hr. After cooling to 0° C., the reaction mixture is quenched with water, extracted with Et2O (5×100 ml), and the combined ether layers is dried over K2CO3. The solvent is removed in vacuo and the residue is purified on silica gel chromatography (eluting 40% ethyl acetate in hexane) to give 2.51 g of 1′-tert-Butoxycarbonyl-2′-methyl-[1,4′]-Bipiperidine, 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208602B2
Source datasetuspto-grants-2007_04
ORD IDord-1042c9a9eeb64aef876584f8a47600ad
Source noteuspto-grants-2007_04