Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Pentane | HCID 8003 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Product | 3-butylfuran | HCID 12224258 | 100% |
Reaction Steps
The iodo-product obtained from Step B above (2.2 g, 8.8 mmol) was dissolved in 60 mL of ether, and stirred in a −78° C. bath. A 1.7 M solution of t-butyllithium in pentane (10.4 mL, 17.7 mmol) was added dropwise. After 20 min, cooling bath was removed. Reaction was continued for 2.5 h, and quenched with H2O (20 mL). The aqueous mixture was stirred overnight and separated. The aqueous layer was extracted with ether (30 mL). The combined organic layers were washed with brine, dried by Na2SO4, and filtered through a Celite pad. Removal of solvent gave 1.10 g (100%) of 3-butylfuran as a reddish-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964646B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-4aca72a60a914c6e9a53ecdf468ef59b |
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| Source note | uspto-grants-2011_06 |
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