HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896917Generated: October 30, 2026
Water → tert-Butyl (3R)-3-formylpiperidine-1-carboxylate
https://huagongshe.com/reaction/896917
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-tert-Butyl 3-ethyl (3R)-piperidine-1,3-dicarboxylate | HCID 1514446 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | tert-Butyl (3R)-3-formylpiperidine-1-carboxylate | HCID 42325667 | 56.5% |
Reaction Steps
A 1.2 M solution of diisobutylaluminum hydride in toluene (30.8 ml, 36.9 mmol) was added at −78° C. to a solution of (3R)-piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (4.13 g, 16.1 mmol) in diethyl ether (30 ml). The reaction mixture was stirred for 2.5 h at −78° C. Water (9.6 ml) was added dropwise. The reaction mixture was warmed to room temperature. The precipitation was removed by filtration through a plug of celite. The celite was washed with tert-butyl methyl ether (3×100 ml). The liquids were combined and dried over magnesium sulfate. The solvent was removed in vacuo, to give 1.94 g of crude (3R)-3-formylpiperidine-1-carboxylic acid tert-butyl ester, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919315B1 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-f4ba397598e74c83b2a4ebcdae08c767 |
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| Source note | uspto-grants-2005_07 |
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