Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Nsc 634137 | HCID 184894 | — |
| Reactant | HCID 89350088 | HCID 89350088 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89368240 | HCID 89368240 | — |
Reaction Steps
A solution of methyl [bis(2,2,2-trifluoroethoxy)phosphoryl]acetate (95%, 9.42 g) in tetrahydrofuran (20 mL) was slowly added to a suspension of sodium hydride (63%, 1.07 g) in tetrahydrofuran (40 mL) with stirring at −30° C. The mixture was stirred at the same temperature for 30 minutes, and bromine (1.46 mL) was then slowly added thereto. After completion of addition, the reaction solution was temporarily heated to −10° C. The reaction solution was cooled to −78° C., and sodium hydride (63%, 1.07 g) was then added thereto at once. The mixture was stirred at the same temperature for 30 minutes, and a solution of the crude product of 4-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3,3-dimethylbutanal (3.59 g) obtained in Step 1 in tetrahydrofuran (20 mL) was then added thereto. The mixture was stirred at −78° C. for 1 hour and then gradually heated to 10° C. over 1 hour with care to prevent foaming. The reaction mixture was further stirred at the same temperature for 1 hour, and an aqueous ammonium chloride solution was then added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with water and saturated sodium chloride solution and dried over anhydrous sodium sulfate. After filtration and concentration under reduced pressure, the obtained crude product was purified by silica gel column chromatography to obtain the title compound (4.53 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946443B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-49758833f0a740a2a1476234b23a5deb |
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| Source note | uspto-grants-2015_02 |
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