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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867364Generated: November 2, 2026

Carbon Dioxide → Tert-butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylate

https://huagongshe.com/reaction/1867364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantPotassium bisulfateHCID 516920—
Reactant1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylateHCID 20585394—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylateHCID 2225892873%

Reaction Conditions

Temperature0 °C

Reaction Steps

6.14 ml (1.2 M in toluene, 7.37 mmol) of DIBALH was dropped to a dry ice cooled (−30° C.) solution of 1.00 g (3.69 mmol) crude 3-methyl-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester in 2 ml of THF. The reaction was warmed up (0° C. for 1 h), continued for 3 h, cooled (−15° C.) and treated again with 0.61 ml (1.2 M in toluene, 0.74 mmol) of DIBALH. After 1 h the reaction was warmed up to 0° C. and neutralized with aqueous 10% KHSO4 solution. The mixture was extracted with ether (3×), the organic phases were washed with a aqueous 10% NaCl solution, dried (Na2SO4) and evaporated to give after flash silica gel column (n-heptane/EtOAc 9:1) 0.61 g (73%) of the title compound as yellow oil. MS: 230.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632829B2
Source datasetuspto-grants-2009_12
ORD IDord-97245c07b29246aea16f31afc06ea9de
Source noteuspto-grants-2009_12