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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976102Generated: October 29, 2026

Iodoacetamide → HCID 19968500, compound

https://huagongshe.com/reaction/976102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoacetamideHCID 3727—
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-BOC-ethylenediamineHCID 187201—
SolventAcetonitrileHCID 6342—
ProductHCID 19968500HCID 1996850055%

Reaction Steps

To a solution of 1.25 g (7.8 mmole) of N-(t-Butoxycarbonyl)ethylenediamine in 10 mL of acetonitrile was added 1.36 mL (7.8 mole) of DIEA followed by 1.44 g (7.8 mmole) of iodoacetamide at room temperature. After 90 min most of the solvent was removed in vacuo and the residue was taken up in 12 mL of CH2Cl2 and was treated with 1.36 mL (7.8 mmole) of DIEA and then 1.1 mL (7.8 mmole) of benzyl chloroformate. The resulting solution was stirred at room temperature for 2 days, and was then concentrated partly in vacuo. The residue was treated with 100 mL of ethyl acetate and 20 mL of 1M aqueous tartaric acid and the layers were separated. The organic layer was washed with 2×15 mL of water, the tartaric acid layer was extracted with 30 mL of ethyl acetate, this extract was washed with 2×10 mL of water, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by flash chromatography on 131 g of silica gel eluting with 2.5 L of 100:4 CH2Cl2: methanol to provide 1.5 g (55%)of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610165
Source datasetuspto-grants-1997_03
ORD IDord-0dcf591d27ec443b94335975e086cad6
Source noteuspto-grants-1997_03