Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 58019861 | HCID 58019861 | — |
| Product | HCID 57663088 | HCID 57663088 | — |
Reaction Steps
The product of example 5 (100 mg) is dissolved in dry THF (3 mL) and cooled to 0° C. under argon. The reagent generated in example 6 (0.72 mL) is added to the reaction flask and the mixture is stirred at 0-5° C. for 1 h and then quenched by addition of 3 M HCl. The mixture is then extracted with ethyl acetate and then dichloromethane and concentrated in vacuo to yield 85 mg. NMR is consistent with structure assignment.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09359360B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-81f7d1a40efd49ca9420c72f491d77e1 |
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| Source note | uspto-grants-2016_06 |
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