Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | HCID 86661510 | HCID 86661510 | — |
| Catalyst | HCID 178479819 | HCID 178479819 | — |
| Product | HCID 57386254 | HCID 57386254 | 86% |
Reaction Steps
A solution of compound (5a) (263.8 mg, 1.106 mmol) and degassed DCM (37) was cooled to −78° C. The flask was flushed with ethylene gas over a period of 10 minutes before ethylene gas was bubbled through the solution itself for 3 additional minutes. Grubbs I catalyst (136.4 mg, 0.1657 mmol) was added and once again ethylene gas was bubbled through the resulting mixture for one minute. The icebath was removed and the mixture stirred for 24 hours. The flask was flushed with argon and the solvent was evaporated. Chromatography of the residue (pentane/ether 200/1) furnished 226.6 mg of compound of (6a) as clear colourless oil with 86% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809395B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-3bc1312c4127483d924f91bc20d389cb |
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| Source note | uspto-grants-2014_08 |
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