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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840599Generated: October 31, 2026

Methanol → tert-Butyl 4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1840599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactanttert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
Producttert-Butyl 4-(hydroxymethyl)-4-methoxypiperidine-1-carboxylateHCID 23447302—

Reaction Steps

To a solution of 6-(tert-butoxycarbonyl)-1-oxa-6-azaspiro[2,5]octane (17.5 g) in methanol (250 ml) was added p-toluene sulfonic acid hydrate (285 mg), and the mixture was stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and to the residue was added ethyl acetate. The mixture was washed with sodium bicarbonate solution and saturated brine, dried and concentrated, and the residue was crystallized from ice-cooled hexane to give colorless solid of 1-(tert-butoxycarbonyl)-4-methoxy-4-piperidinemethanol (9.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680312B2
Source datasetuspto-grants-2004_01
ORD IDord-9332446a54b74d31b0c6b49623af784c
Source noteuspto-grants-2004_01