HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2092007Generated: October 29, 2026
Cyclohexene oxide → rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanol
https://huagongshe.com/reaction/2092007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexene oxide | HCID 9246 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Solvent | Water | HCID 962 | — |
| Product | rel-(1R,2R)-2-(1-Pyrrolidinyl)cyclohexanol | HCID 10103566 | 98% |
Reaction Steps
Pyrrolidine (4.26 g, 60 mmol) was added to a solution of cyclohexene oxide (1.96 g, 20 mmol) in H2O (6 mL), and the resulting mixture was heated at 90° C. for 16 hours. After cooling, the solvent was removed under reduced pressure and the resulting residue was extracted with DCM (10 mL×3). The organic phasew were combined and dried with anhydrous Na2SO4. After removing the Na2SO4 by filtration, the solvent was evaporated and the material dried under vacuum to afford the desired compound (+/−)-1 (3.3 g, 19.5 mmol, yield 98%). 1H NMR (CDCl3) δ 4.06 (s, 1H), 3.45-3.30 (m, 1H), 2.75-2.63 (m, 2H), 2.62-2.50 (m, 2H), 2.51-2.42 (m, 1H), 1.90-1.58 (m, 8H), 1.45-1.15 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08440687B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-be52d69043234f07bab0cf5546b4b55b |
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| Source note | uspto-grants-2013_05 |
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