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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | 1-tert-Butyl 3-ethyl 3-methylpiperidine-1,3-dicarboxylate | HCID 20585394 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-(hydroxymethyl)-3-methylpiperidine-1-carboxylate | HCID 22258928 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632829B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-97245c07b29246aea16f31afc06ea9de |
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| Source note | uspto-grants-2009_12 |
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