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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255482Generated: October 28, 2026

Sodium Carbonate → Carbamic acid, [3-[(cyanomethyl)amino]propyl]-, 1,1-dimethylethyl ester

https://huagongshe.com/reaction/2255482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBromoacetonitrileHCID 11534—
Reactanttert-Butyl (3-aminopropyl)carbamateHCID 2735700—
SolventEthanolHCID 702—
ProductCarbamic acid, [3-[(cyanomethyl)amino]propyl]-, 1,1-dimethylethyl esterHCID 1056054655%

Reaction Steps

A solution of (3-aminopropyl)carbamic acid 1,1-dimethylethyl ester (6.00 g, 34 mmol), prepared by the method of Saari et al., J. Med. Chem., 33, 97 (1990), in absolute ethanol (90 mL) was treated with sodium carbonate (3.96 g, 37 mmol) followed by a solution of bromoacetonitrile (2.6 mL, 37 mmol) in ethanol (30 mL) over 45 min. After stirring at room temperature overnight, the contents of the flask were filtered, preadsorbed onto silica gel, and purified by flash chromatography (7 cm diameter, elution with 2.5% methanol in dichloromethane) to afford [3-(cyanomethylamino)propyl]carbamic acid 1,1-dimethylethyl ester as a yellow oil (3.99 g, 55%); IR (neat, cm-1): 3330, 2240, 1700; MS (+CI): 214 (MH+, 20), 187 (76), 158 (100), 131 (44); 1H NMR (CDCl3, 400 MHz): δ 4.80 (br s, NH), 3.61 (s, 2H), 3.22 (q, J=6.5 Hz, 2H), 2.79 (t, J=6.5 Hz, 2H), 1.69 (p, J=6.5 Hz, 2H), 1.45 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240946
Source datasetuspto-grants-1993_08
ORD IDord-72e7810556ef4942957817f4c628023f
Source noteuspto-grants-1993_08