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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919715Generated: November 2, 2026

Dimethyl Sulfate → N-Boc-2-Methyl-Piperidine

https://huagongshe.com/reaction/1919715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantN-(tert-butoxycarbonyl)piperidineHCID 7010304—
ReactantCID 53628100HCID 178418400—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductN-Boc-2-Methyl-PiperidineHCID 457807799.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of N-Boc-Piperidine (15.0 g, 80.95 mmol) in ether (160 mL) was cooled to −78° C. and treated with TMEDA (15.9 mL, 105.2 mmol) followed by sec-BuLi (85 mL, 105.2 mmol) dropwise. The mixture was stirred for 3 h at −78° C. and then treated with a solution of dimethyl sulfate (15.3 mL, 161.9 mmol) in 65 mL of ether. The mixture was warmed to room temperature and then was diluted with water and extracted with ether. The combined extracts were dried over K2CO3 and then concentrated to give a crude product as a colorless oil. The product was purified by column chromatography on silca gel with 5% EtOAc/hexane to afford 16.0 g (81%) of product as a clear oil which was homogeneous by TLC analysis. 1H NMR (300 MHz) δ 4.33 (m, 1H), 3.92-3.81 (pair of br. d, 1H), 2.81-2.72 (dt, 1H), 1.60-1.36 (m, 15H), 1.09-1.07 (d, 3H); 13C NMR (75 MHz) 154.9 (s), 78.6 (s), 45.9 (s), 38.6 (s), 29.9 (s), 28.4 (s), 25.6 (s), 18.6 (s), 15.6 (s) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168657B2
Source datasetuspto-grants-2012_05
ORD IDord-9a39cc02c7094effb012a6d7b684552b
Source noteuspto-grants-2012_05