Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzyl bromide | HCID 68021 | — |
| Reactant | 3-Hydroxy-hexahydro-pyrrolo[3,2-b]pyrrole-1,4-dicarboxylic acid 4-benzyl ester 1-tert-butyl ester | HCID 67607394 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67609216 | HCID 67609216 | 94.4% |
Reaction Steps
Bicyclic alcohol 43 (4.2 g, 11.59 mmol) and 4-fluoro-benzyl bromide (2.2 mL, 17.4 mmol) were dissolved in DMF (115 mL) and cooled to 0° C. Sodium hydride (930 mg, 23.2 mmol) was added and, after ˜5 min, the ice bath was removed. After 15 min, the reaction mixture was diluted with toluene (250 mL) and saturated aqueous NH4Cl (500 mL) and extracted with 1:1 Et2O/hexanes (600 mL). The organic layer was washed successively with 1N HCl, water, saturated aqueous NaHCO3, water, and brine, dried over anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by flash silica gel chromatography (10:1 to 1:1 hexanes/EtOAc) to afford 5.15 g of 44 as a viscous oil (94%): 1H NMR (300 MHz, CDCl3): δ7.36 (m, 6H), 7.07-6.92 (m, 3H), 5.15 (m, 2H), 4.63 (m, 1H), 4.50 (m, 1H), 4.32 (m, 1H), 4.19 (m, 1H), 3.97 (m, 1H), 3.87-3.64 (m, 2H), 3.25-3.08 (m, 2H), 2.35 (m, 0.5H), 2.17 (m, 0.5H), 1.88 (m, 1H), 1.46 (s, 9H) ppm. Mass spectrum, m/z [414.7] (M−t-Bu)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415486B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-451f9d00365d412da3a4c8ed13bd660a |
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| Source note | uspto-grants-2013_04 |
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