HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749991Generated: October 30, 2026
Water → tert-butyl (2R)-2-(hydroxymethyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/749991
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (2R)-1-[(tert-butoxy)carbonyl]piperidine-2-carboxylic acid | HCID 688618 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-butyl (2R)-2-(hydroxymethyl)piperidine-1-carboxylate | HCID 6933953 | 99.1% |
Reaction Steps
To a solution of (R)-Piperidine-1,2-dicarboxylic acid 1-tert-butyl ester (5 g, 21.8 mmol) in anhydrous THF (32 mL) at 0-5° C. was added borane-tetrahydrofuran complex (1M solution in THF) (3.6 g, 41.84 mmol) over a period of 15 min. The mixture was stirred at 0-5° C. for 2 h and then at rt for 2 h. The mixture was added over a period of 10 min to cold water (75 mL) and extracted with EtOAc (300 mL). The aqueous layer was re-extracted with EtOAc (2×150 mL). The organic layers were combined, dried over anhydrous Na2SO4 and concentrated to obtain the title product as a colorless oil (4.65 g., 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402684B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-b87738e6685748d0a0f579470ae564d5 |
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| Source note | uspto-grants-2008_07 |
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