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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221467Generated: November 1, 2026

p-Fluorophenethylamine → (s)-{[(4-Fluorobenzyl)methylcarbamoyl]phenylmethyl}carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2221467

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluorophenethylamineHCID 4653—
ReactantPyBroPHCID 2733179—
Reactant(2R)-2-{[(tert-butoxy)carbonyl]amino}-2-phenylacetic acidHCID 2755953—
SolventDichloromethaneHCID 6344—
Product(s)-{[(4-Fluorobenzyl)methylcarbamoyl]phenylmethyl}carbamic acid tert-butyl esterHCID 6926774396%

Reaction Steps

A solution of N-Boc-L-phenylglycine (H, 17.2 g, 68.5 mmol) and (4-fluorobenzyl)methylamine (10.47 g, 75.3 mmol) in CH2Cl2 (550 mL) was cooled to 0° C. Disopropylethylamine (35.8 mL, 205 mmol) and PyBroP (38.3 g, 82.1 mmol) were then added sequentially. The cooling bath was removed and the reaction mixture was stirred at room temperature overnight. The solvent was evaporated and the title compound (24.5 g, 96%) was isolated by chromatography on silica gel eluting with a gradient of 40% to 60% ethyl acetate in hexane. 1H NMR (selected signals, CDCl3): □6.02 (d, 0.3H), 5.56 (d, 0.7H), 2.83 (s, 0.9H), 2.78 (s, 2.1H), 1.40 (s, 6.3 H, 1.39 (s, 2.7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368573B2
Source datasetuspto-grants-2008_05
ORD IDord-d7c7c852f91c4e6c8b43812366c65384
Source noteuspto-grants-2008_05