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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045377Generated: October 31, 2026

Acetic Anhydride → N'-(acetyloxy)-4-iodobenzenecarboximidamide

https://huagongshe.com/reaction/1045377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantN-Hydroxy-4-iodo-benzamidineHCID 4429393—
SolventDichloromethaneHCID 6344—
SolventDiisopropyl EtherHCID 7914—
ProductN'-(acetyloxy)-4-iodobenzenecarboximidamideHCID 86663308—

Reaction Steps

To a suspension of the product obtained in Step A above (8.43 g, 32.17 mmol) in 200 ml of CH2Cl2 there are added 6.72 ml (48.2 mmol) of triethylamine. 3.34 ml (35.4 mmol) of acetic anhydride are added dropwise and the solution is stirred overnight at ambient temperature. After washing 3 times with water and then with brine, the organic phase is dried over MgSO4 and evaporated. The solid obtained is taken up in isopropyl ether and then filtered to yield the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569285B2
Source datasetuspto-grants-2013_10
ORD IDord-8dc8ac9c5a664b2bb408d871c4126b8e
Source noteuspto-grants-2013_10