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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179136Generated: October 29, 2026

Benzamide → N-(2-methoxyphenyl)benzamide

https://huagongshe.com/reaction/2179136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzamideHCID 2331—
Reactanto-IodoanisoleHCID 68257—
ProductN-(2-methoxyphenyl)benzamideHCID 22040721%

Reaction Steps

Using general procedure A, benzamide (150 mg, 1.24 mmol) was coupled with 2-iodoanisole (135 μL, 1.04 mmol) at 40° C. for 18 h. The crude product was purified by flash chromatography on silica gel (2×15 cm; hexane-ethyl acetate 3:1; 15 mL fractions). Fractions 8-12 provided 49 mg (21% yield) of the product as a colorless oil. The 1H NMR spectrum was in accord with that reported by Narasaka et al. Tsutsi, H.; Ichikawa, T.; Narasaka, K. Bull. Chem. Soc. Jpn. 1999, 72, 1869.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067955B2
Source datasetuspto-grants-2015_06
ORD IDord-414c773638c14c39827b536f41f0a68c
Source noteuspto-grants-2015_06