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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419335Generated: October 25, 2026

Chloroacetyl chloride → N'-(chloroacetyl)-3-(methyloxy)-4-nitrobenzohydrazide

https://huagongshe.com/reaction/419335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant3-Methoxy-4-nitrobenzohydrazideHCID 21883875—
SolventEthyl AcetateHCID 8857—
ProductN'-(chloroacetyl)-3-(methyloxy)-4-nitrobenzohydrazideHCID 5945289264%

Reaction Steps

To 3-(methyloxy)-4-nitrobenzohydrazide (3.65 g, 17.3 mmol) in EtOAc (150 mL) was added chloroacetyl chloride (1.50 mL, 18.8 mmol). The reaction was stirred open to air overnight. The solid was filtered and washed with diethyl ether to provide the title compound (3.17 g, 11.0 mmol, 64%). 1H NMR (400 MHz, DMSO-d6) δ ppm 3.98 (s, 3H), 4.21 (s, 2H), 7.56 (dd, J=8.2, 1.6 Hz, 1H), 7.74 (d, J=1.8 Hz, 1H), 7.99 (d, J=8.1 Hz, 1H), 10.48-10.54 (m, 1H), 10.82 (d, J=1.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093239B2
Source datasetuspto-grants-2012_01
ORD IDord-745fc27ce7ca455fa04f08fd189a966d
Source noteuspto-grants-2012_01