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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278470Generated: November 1, 2026

Water → 3,5-diiodo-N'-(3-methoxybenzoyl)benzohydrazide

https://huagongshe.com/reaction/2278470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactantm-Anisoyl chlorideHCID 74374—
ReactantN-hydroxy-3,5-diiodobenzamideHCID 67511905—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
Product3,5-diiodo-N'-(3-methoxybenzoyl)benzohydrazideHCID 67510313—

Reaction Steps

To a solution of 3,5-Diiodobenzohydrazide (4.5 g, 11.60 mmol) in dry THF/DMF (100.0 ml:24.0 ml) was slowly added 3-methoxybenzoyl chloride (2.2 g, 12.90 mmol) at 0° C. under nitrogen. After addition of 3-methoxybenzoyl chloride, the reaction was warmed up to room temperature. The reaction mixture was stirred for 19 hours at room temperature and then pyridine (5.0 ml) was added and stirred for additional 1 h. Water (300.0 ml) was added to reaction mixture. The white solid was obtained and collected by filtration. After dried under vacuum, product was obtained as white powder in 5.05 g (83.3%). 1H NMR (400 MHz, DMSO-d6, δ): 10.72 (s, 1H, NH), 10.62 (s, br, 1H, NH), 8.33 (t, J=1.6 Hz, 1H), 8.23 (d, J=1.6 Hz, 2H), 7.50-7.41 (m, 3H), 7.15 (m, 1H), 3.81 (s, 3H, OCH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133177B2
Source datasetuspto-grants-2015_09
ORD IDord-b72c713bb11f4898a07b321f1c42bd27
Source noteuspto-grants-2015_09