HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → [1-(5-Iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | tert-Butyl (1-(furan-2-yl)cyclopropyl)carbamate | HCID 67117129 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium Thiosulfate | HCID 24477 | — |
| Product | [1-(5-Iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester | HCID 67115732 | 72.7% |
Reaction Steps
To a solution of (1-furan-2-yl-cyclopropyl)-carbamic acid tert-butyl ester (4.30 g, 19.3 mmol) in anhydrous DMF (77 mL) at room temperature was added N-iodosuccinimide (4.77 g, 21.2 mmol) as a solid in one portion. The reaction was stirred for 2.5 h over which time a deep red color developed. The reaction was diluted with sat. aq. Na2S2O3 (75 mL), water (75 mL), and diethyl ether (100 mL). The layers were separated and the aqueous layer was extracted with diethyl ether (2×100 mL). The combined organic layers were dried over Na2SO4 and concentrated. The resultant solids were triturated with hexanes to give 4.9 g [1-(5-iodo-furan-2-yl)-cyclopropyl]-carbamic acid tert-butyl ester as a light yellow powder, m/z 350.5 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575360B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-55af917f52c4430ca644bccc249ddb0d |
| Source note | uspto-grants-2013_11 |