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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527385Generated: October 31, 2026

Trifluoroacetic acid → (9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate

https://huagongshe.com/reaction/527385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 131730600HCID 131730600—
SolventDichloromethaneHCID 6344—
Product(9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamateHCID 1145033899.9%

Reaction Steps

TFA (55.30 mL, 717.76 mmol, 15.0 eq) was added at 0° C. to a stirred solution of (tert-butoxy)-N-{4-[(fluoren-9-yl-methoxy)carbonylamino]phenyl}carboxamide (20.60 g, 47.85 mmol, 1.0 eq) in CH2Cl2 (900 mL). The resulting solution was allowed to come at room temperature. After stirring overnight at room temperature, the reaction mixture was concentrated to dryness and the residue was triturated in water. Then the mixture was filtered to afford 15.80 g of the expected crude product as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346799B2
Source datasetuspto-grants-2016_05
ORD IDord-99f524d309bc41718bcb41e42f20fd6b
Source noteuspto-grants-2016_05