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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254374Generated: October 30, 2026

Triethylamine → {4-[4-(Carbamoylmethylamino)phenyl]butyl}carbamic acid tert-butyl ester

https://huagongshe.com/reaction/254374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoacetamideHCID 69632—
Reactant[4-(4-Aminophenyl)butyl]carbamic acid tert-butyl esterHCID 11558019—
CatalystHCID 178418647HCID 178418647—
SolventDimethylformamideHCID 6228—
Product{4-[4-(Carbamoylmethylamino)phenyl]butyl}carbamic acid tert-butyl esterHCID 5866481622%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of [4-(4-aminophenyl)butyl]carbamic acid tert-butyl ester (0.8 g, 3.03 mmol), 2-bromoacetamide (0.46 g, 3.33 mmol), triethylamine (0.2 mL, 3.33 mmol), and DMF (30 mL) was stirred at 80° C. for 20 hours. TLC indicated that the reaction was not complete. Silver carbonate (0.92 g, 3.33 mmol) was thus added. The reaction was further stirred at 80° C. for 24 hours. The reaction mixture was passed through a silica plug. The solvent was evaporated in vacuo. The residue was purified by flash chromatography (silica gel, 3:1 ethyl acetate/dichloromethane, v/v) to provide 390 (0.20 g, 22%) as a white solid. 1H NMR (300 MHz, CD3OD) δ 1.42 (s, 9H), 1.55 (m, 4H), 2.50 (t, 2H), 3.03 (t, 2H), 3.70 (s, 2H), 6.52 (d, 211), 7.00 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875619B2
Source datasetuspto-grants-2011_01
ORD IDord-cb3e05fbd37642798c107f34bfedde25
Source noteuspto-grants-2011_01