Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166445Generated: October 28, 2026

Ethylenediamine → N-BOC-ethylenediamine

https://huagongshe.com/reaction/1166445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantDimethylformamideHCID 6228—
Reactantt-Butyl-p-nitrophenyl carbonateHCID 67297514—
ProductN-BOC-ethylenediamineHCID 18720163%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl-4-nitrophenyl carbonate (1, 10 g, 0.0418 mol) dissolved in DMF (50 mL) was added dropwise over a period of 30 minutes to a solution of ethylenediamine (27.9 mL, 0.418 mol) and DMF (50 mL) and stirred overnight. The mixture was evaporated to dryness in vacuo, and the resulting oil dissolved in water (250 mL). After cooling to 0° C., the pH was adjusted to 3.5 with 4 M hydrochloric acid. The solution was then filtered and extracted with chloroform (3×250 mL). The pH was adjusted to 12 (at 0° C.) with 2 M sodium hydroxide, and the aqueous solution extracted with methylene chloride (3×300 mL). After treatment with a solution of saturated aqueous sodium chloride (250 mL), the methylene chloride solution was dried over magnesium sulfate. After filtration, the solution was evaporated to dryness in vacuo, resulting in 4.22 g (63%) of the product as an oil. 1H-NMR (90 MHz, CDCl3) δ: 1.44 (s, 9H); 2.87 (t, 2H); 3.1 (q, 2H); 5.62 (sb).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613873B1
Source datasetuspto-grants-2003_09
ORD IDord-b504b5288c9849d68ade556358fc1aec
Source noteuspto-grants-2003_09