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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641775Generated: November 1, 2026

Methyl iodide → 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester

https://huagongshe.com/reaction/1641775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMethyl N-Boc-4-piperidinepropionateHCID 1502093—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventTetrahydrofuranHCID 8028—
Product2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl esterHCID 59261070—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester (2.0 g, 7.38 mmol) from above was dissolved in tetrahydrofuran (50 mL). The solution was cooled to −78° C. and sodium bis(trimethylsilyl)amide (1.0 M, 9.0 mL) was added. The mixture was stirred at −78° C. for 1 hr and methyl iodide (1.2 mL, 19.5 mmol) was added. The mixture was warmed to room temperature and stirred for 2 hrs. The mixture was extracted with ether and washed with dilute hydrochloric acid. The organic layer was dried, filtered and concentrated. The residue was purified using flash chromatography (eluting with ethyl acetate and hexanes) to give 2-methyl-3-(N-Boc-piperidine-4-yl)-propionic acid methyl ester as an oil (789 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08115011B2
Source datasetuspto-grants-2012_02
ORD IDord-44587313d66a4a58b9933e8e615839e6
Source noteuspto-grants-2012_02