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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168194Generated: October 31, 2026

Methyl iodide → 1-Boc-3,4,4-trimethoxypiperidine

https://huagongshe.com/reaction/2168194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTert-butyl 3-hydroxy-4,4-dimethoxypiperidine-1-carboxylateHCID 11425480—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-3,4,4-trimethoxypiperidineHCID 59263089—

Reaction Steps

To a solution of 1,1-dimethylethyl 3-hydroxy-4,4-bis(methyloxy)-1-piperidinecarboxylate D16 (11 g) in THF (150 ml) was added Potassium t-Butoxide (23.5 g, 210 mmol) at 0° C. The reaction mixture was stirred for 20 mins and the methyliodide (5.2 ml, 84 mmol) was added. The reaction mixture was allowed to warm up to room temperature and stirred overnight. The resulting mixture was concentrated and dissolved in EtOAc and washed with water. The organic layer was concentrated in vacuo to obtain crude product. Product was purified on silica gel eluting with DCM/MeOH 50/1 to obtain the desired product D17 as a yellow oil in 5 g. LCMS [MH+] [email protected] min (5 min run)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045485B2
Source datasetuspto-grants-2015_06
ORD IDord-648aa14ff4da4d168dbc693d25cf26db
Source noteuspto-grants-2015_06