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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841043Generated: October 31, 2026

Benzamide → 3-iodo-4-methylbenzamide

https://huagongshe.com/reaction/841043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamideHCID 2331—
ReactantAmmonium HydroxideHCID 14923—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Iodo-4-methylbenzoic acidHCID 621640—
Product3-iodo-4-methylbenzamideHCID 83332993%

Reaction Steps

3-Iodo-4-methyl benzoic acid was converted to the corresponding benzamide according to the procedure described for compound la above ((COCl)2, NH4OH), to provide 3-iodo-4-methyl benzamide in 93% yield. Further conversion according to Method B described above provided compound 10 in 48% yield. 1H NMR (CDCl3) δ 8.02 (1 H, d, J=1.6 Hz), 7.95 (1 H, d, J=7.9 Hz), 7.29 (1 H, d, J=7.9 Hz), 6.46 (1 H, d, J=15.9 Hz), 6.10 (1 H, br s), 5.75 (1 H, br s), 4.08 (2 H, q, J=7.1 Hz), 2.48 (3 H, s), 1.42 (3 H, t, J=7.1 Hz) Anal. (C13H12N2O3.0.2 H2O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369226B1
Source datasetuspto-grants-2002_04
ORD IDord-cf0986c8f7fd4d35ae9436f9f5a80dc8
Source noteuspto-grants-2002_04