HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(Tert-butoxycarbonylamino)-5-phenoxyindan
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22719625 | HCID 22719625 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(Tert-butoxycarbonylamino)-5-phenoxyindan | HCID 22719586 | 90% |
Reaction Steps
2-(tert-butoxycarbonylamino)-5-hydroxyindan (100 mg, 0.40 mmol) synthesized in the above Reference Production Example 1 was dissolved in acetone (2 ml), to which potassium carbonate (58 mg, 0.45 mmol) and benzylbromide (48 μl, 0.40 mmol) were added, and the mixture was heated to reflux for 3 hours. The reaction mixture was extracted with ether and dried, and then the solvent was distilled off under reduced pressure to obtain 2-(tert-butoxycarbonylamino)-5-phenoxyindan (120 mg, 0.36 mmol) having the following physical properties:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06703421B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-053fc30e6b724abc8a11c9c550411c9f |
| Source note | uspto-grants-2004_03 |