Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 53734908 | HCID 53734908 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54248970 | HCID 54248970 | — |
Reaction Steps
7 ml (7 mmol) of a molar solution of BH3 /THF are added, dropwise and with vigorous stirring, to a solution, maintained under nitrogen, of 1.20 g (2.70 mmol) of the compound obtained in Step 3 (diastereoisomer 1) in 30 ml of anhydrous THF. The mixture is then heated at 70° C. for 1 hour and is then cooled, treated with 8 ml of CH3OH and stirred at 20° C. for 1 hour. After concentrating in vacuo, the residue is chromatographed on silica, eluting with a solution of CH2Cl2 /CH3OH=95/5, to yield the title compound in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06127396 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-de7e066230be4c9b9236dd36bd8dd415 |
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| Source note | uspto-grants-2000_10 |
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