Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178448306 | HCID 178448306 | — |
| Catalyst | Cuprous chloride | HCID 62652 | — |
| Product | HCID 68032719 | HCID 68032719 | — |
Reaction Steps
To a 0° C. solution of butenyl magnesium chloride (45.6 mL, 0.5 M) was added copper(I) chloride (0.113 g) followed by methylcyclopropane oxide (1.12 g) in diethyl ether (5 ml). The reaction mixture was warmed to room temperature and stirred for 20 hours. The mixture was cooled back to 0° C. before pouring into a saturated solution of ammonium chloride (at 0° C.). The mixture was extracted with ethyl acetate (3×). The combined organic fractions were dried over magnesium sulfate, filtered and concentrated carefully. The residue was purified by flash chromatography (ISCO, 0 to 30% ethyl acetate in hexanes) to give the desired product (1.3 g). 1H NMR (400 MHz, CDCl3): δ (ppm) 5.86-5.79 (m, 1H), 5.05-4.99 (m, 1H), 4.97-4.93 (m, 1H), 2.20-2.09 (m, 1H), 2.02-1.92 (m, 2H), 1.73-1.50 (m, 7H), 1.31-1.10 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328138B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-c2e23f2164164277b63e6fd2a2ac1aa1 |
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| Source note | uspto-grants-2016_05 |
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