HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → (9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 131730600 | HCID 131730600 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate | HCID 11450338 | 99.9% |
Reaction Steps
TFA (55.30 mL, 717.76 mmol, 15.0 eq) is added at 0° C. to a stirred solution of (tert-butoxy)-N-{4-[(fluoren-9-ylmethoxy)carbonylamino]phenyl}carboxamide (20.60 g, 47.85 mmol, 1.0 eq) in CH2Cl2 (900 mL). The resulting solution is allowed to warm to room temperature. After stirring overnight at room temperature, the reaction mixture is concentrated to dryness and the residue is triturated in water. Then the mixture is filtered to afford 15.80 g of the expected crude product as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08877961B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-e0cb00e501a947efa5abeaf6a020cfad |
| Source note | uspto-grants-2014_11 |