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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339959Generated: October 30, 2026

Ammonium Acetate → Tert-butyl 2-amino-2-(3-fluorophenyl)ethylcarbamate

https://huagongshe.com/reaction/339959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactanttert-butyl N-[2-(3-fluorophenyl)-2-oxoethyl]carbamateHCID 84173790—
SolventMethanolHCID 887—
ProductTert-butyl 2-amino-2-(3-fluorophenyl)ethylcarbamateHCID 7685377494%

Reaction Steps

To a flask were added tert-butyl[2-(3-fluorophenyl)-2-oxoethyl]carbamate (0.32 g, 1.3 mmol) and ammonium acetate (2.02 g, 26.2 mmol) and methanol (10 mL) and sodium cyanoborohydride (0.22 g, 3.5 mmol). The mixture was refluxed for 2 h. The solvent was removed under vacuum. To the residue was added EtOAc and 50 mL of 1M NaOH. The aqueous phase was extracted again with fresh EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and dried under vacuum to give 0.301 g (94% yield) of the final product as oil. LC-MS found: 155.1 (M−Boc)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895571B2
Source datasetuspto-grants-2014_11
ORD IDord-ea277ebecd2a4704bf0fe33706cb0ab8
Source noteuspto-grants-2014_11