Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Diethyl 4-methyleneheptanedicarboxylate | HCID 86634462 | — |
| Reactant | HCID 178443585 | HCID 178443585 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67191093 | HCID 67191093 | 99% |
Reaction Steps
24.5 ml (24.5 mmol) of 1.0 M diethyl zinc/hexane solution was added to 30 ml of dichloromethane, and then a solution of 1.89 ml (24.5 mmol) of trifluoroacetic acid in 10 ml of dichloromethane was added with stirring under ice-cooling. The reaction solution was stirred for 20 minutes at the same temperature, then a solution of 1.97 ml (24.5 mmol) of diiodomethane in 10 ml of dichloromethane was added and stirred for 20 minutes, and 1.40 g (6.13 mmol) of a solution of diethyl 4-methyleneheptanedicarboxylate (compound described in J.A.C.S. 107, 13, 3981-3997 (1985)) in 10 ml of dichloromethane was further added. After the reaction solution was stirred for 6 hours at room temperature, ice water was added to the reaction solution and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography (solvent; hexane:ethyl acetate=5:1) to give 1.48 g of the title compound as a brown oil (yield: 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935835B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-bbe61f53495e4983b81bb8c8d9aceb0a |
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| Source note | uspto-grants-2011_05 |
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