Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexene oxide | HCID 9246 | — |
| Reactant | Thiazolidine | HCID 10444 | — |
| Reactant | Magnesium perchlorate | HCID 24840 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 16735232 | HCID 16735232 | 47% |
Reaction Steps
To anhydrous magnesium perchlorate (12.93 g, 53.3 mmol) was added a solution of cyclohexene oxide (6.1 mL, 58.6 mmol) in anhydrous acetonitrile (25 mL) and the resulting mixture was stirred at room temperature for 20 min. Then a solution of thiazolidine (5.16 g, 55.0 mmol) in anhydrous acetonitrile was added and the reaction mixture was heated at 35° C. for 16 hours. The reaction mixture was concentrated in vacuo and the residue was partitioned between water (350 mL) and diethyl ether (350 mL). The aqueous layer was separated and extracted once more with diethyl ether (350 mL). The combined organic extracts were dried over sodium sulfate and concentrated in vacuo to provide the crude product. The crude aminoalcohol was purified by dry-column chromatography with a mixture of ethyl acetate-hexanes (1:1, v/v) as eluent to yield 4.83 g (47% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008342B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-81c4418d237b4a4ea6ce2aa799d6db25 |
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| Source note | uspto-grants-2011_08 |
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