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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596042Generated: October 29, 2026

Dimethylformamide → (S)-2-amino-2-(3-fluoro-5-iodophenyl)ethyl di-tert-butyl phosphate

https://huagongshe.com/reaction/596042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPiperidineHCID 8082—
Reactant(9H-fluoren-9-yl)methyl piperidine-1-carboxylateHCID 21896484—
Reactant(S)-(9H-fluoren-9-yl)methyl (2-((di-tert-butoxyphosphoryl)oxy)-1-(3-fluoro-5-iodophenyl)ethyl)carbamateHCID 118054603—
SolventEthyl AcetateHCID 8857—
Product(S)-2-amino-2-(3-fluoro-5-iodophenyl)ethyl di-tert-butyl phosphateHCID 118045308—

Reaction Steps

To (S)-(9H-fluoren-9-yl)methyl (2-((di-tert-butoxyphosphoryl)oxy)-1-(3-fluoro-5-iodophenyl)ethyl)carbamate (6450 mg, 9.27 mmol) was added DMF (Volume: 90 mL) followed by piperidine (25 mL, 253 mmol) and stirred at room temperature for 30 minutes, followed by LCMS. To the crude reaction mixture was added 750 ml of ethyl acetate, washed with saturated sodium bicarbonate (2×), water (5×), saturated salt solution, dried sodium sulfate, and filtered. The solvent was concentrated off to constant mass under high vacuum to give the desire crude product which includes FMOC piperidine impurity, used as is. LCMS (m/z): 474.2 (MH+), 0.80 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-19e6287ad4b94eaaa8dc70079e006e6c
Source noteuspto-grants-2016_01