Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromomethane | HCID 3024 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 4-Iodobenzaldehyde | HCID 96657 | — |
| Reactant | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| Reactant | HCID 21250577 | HCID 21250577 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | Zinc Sulfate | HCID 24424 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21250649 | HCID 21250649 | — |
Reaction Steps
Zinc dust (253 mg) was stirred under nitrogen overnight. To this was added DMF (5 ml) and dibromomethane (55 mg) dissolved in DMF (1 ml) and the mixture warmed to ˜70° C. The reaction mixture was cooled to room temperature and chlorotrimethylsilane (32 mg) in DMF (1 ml) added and stirred at room temperature for 15 minutes. To this was added 2-iodo-N-Boc-azetidine (Billotte, S., Synlett, 1998, 379-380) (1.04 g) in DMF (5 ml). The reaction mixture warmed to 40° C. and the mixture sonicated for 30 minutes during which time the zinc powder dissolved to leave a hazy solution. To the solution of zincate was added 4-iodobenzaldehyde (Preparation 43) (851 mg in 5 ml DMF), tri-2-furylphosphine (35 mg in 1 ml DMF) and Pd(dbq)2 (42 ml in 1 ml DMF). The resulting mixture was heated at 60-70° C. for 4 hours, cooled to room temperature and partitioned between ammonium chloride solution and diethyl ether, and the aqueous layer was extracted with diethyl ether (3×). The combined organic extracts were dried (Na2SO4), evaporated in vacuo and purified over silica (pentane:ethyl acetate; 4:1) to afford the title compound as a mobile oil, 626 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06200978B1 |
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| Source dataset | uspto-grants-2001_03 |
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| ORD ID | ord-323e4c0949d04e15b5122a2b3f798784 |
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| Source note | uspto-grants-2001_03 |
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