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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443303Generated: October 30, 2026

Methanol → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/443303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoraneHCID 6331—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—

Reaction Steps

To a solution of N-t-butoxycarbonyl isonipecotic acid (15.0 g, 65.4 mmol) from example 3 step A, in anhydrous THF (50 ml), was added borane (65.4 ml of a 1M solution in THF, 65.4 mmol) at room temperature. After 72 hours methanol (50 ml) was added and the solvent evaporated in vacuo. The residue was dissolved in methanol (100 ml) and the solvent evaporated in vacuo. The eesidue was partitioned between EtOAc and NaHCO3, the organic layer separated and washed with brine, dried (MgSO4) and evaporated in vacuo. The residue was purified by chromatography (Silica gel, eluting with 50% EtOAc in hexanes ) to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891889
Source datasetuspto-grants-1999_04
ORD IDord-c6b55d105ed94c3780a4253db0d4a856
Source noteuspto-grants-1999_04