Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 19380957 | HCID 19380957 | — |
| Product | HCID 86749014 | HCID 86749014 | 45% |
Reaction Steps
To a stirred solution of 19 (325 mg, 1.1 mmol) in THF (5 mL) at -78° C. was added LDA (0.5M in THF 2.4 mL) dropwise. After 15 min allyl bromide (0.16 mL, 2.2 mmol) was added and the reaction stirred at -78° C. for 1 hr followed by quenching with HOAc (0.1 mL). The reaction mixture was then diluted with ethyl acetate and then washed with water and brine, dried (MgSO4), and concentrated. Flash chromatography (silica gel, 50% ethyl acetate/hexanes) gave 20 (160 mg, 45%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455243 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-824a3fdf25d2420eb2bae97b744570d0 |
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| Source note | uspto-grants-1995_10 |
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