HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → Tert-butyl(trans)-2-{4-[(4-cyanobenzyl)oxy]phenyl}cyclopropylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Bromomethyl)benzonitrile | HCID 86996 | — |
| Reactant | tert-Butyl N-[(1R,2S)-rel-2-(4-hydroxyphenyl)cyclopropyl]carbamate | HCID 86672576 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Tert-butyl(trans)-2-{4-[(4-cyanobenzyl)oxy]phenyl}cyclopropylcarbamate | HCID 86672578 | 71.3% |
Reaction Steps
4-(bromomethyl)benzonitrile (0.47 g, 2.40 mmol) was added to a mixture of Intermediate J, tert-butyl(trans)-2-(4-hydroxyphenyl)cyclopropylcarbamate, (0.50 g, 2.00 mmol), K2CO3 (0.42 g, 3.00 mmol) and NaI (0.03 g, 0.20 mmol) in acetone (15 mL) and stirred at room temperature for 3 d. After removal of the solvent, the crude residue was dissolved in EtOAc (30 mL) and washed with brine (2×25 mL). The organic layer was dried over anhydrous Na2SO4 and filtered. After removal of the solvent, the residue was purified by column chromatography on silica gel (5%-50% EtOAc/Hexanes), affording 0.52 g of tert-butyl(trans)-2-{4-[(4-cyanobenzyl)oxy]phenyl}cyclopropylcarbamate [Rf=0.2 (30% EtOAc/Hexanes), pale yellow solid, 71% yield].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946296B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-8ac8e857a20741048ef653797243f3f1 |
| Source note | uspto-grants-2015_02 |