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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427654Generated: October 25, 2026

Triethylamine → n-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamide

https://huagongshe.com/reaction/427654

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantN-(4-Methoxyphenyl)-2-hydroxybenzamideHCID 478806—
SolventDichloromethaneHCID 6344—
Productn-(4-Methoxyphenyl)-2-(4-tert-butylbenzoyloxy)benzamideHCID 1817441761%

Reaction Steps

To a solution of N-(4-methoxyphenyl)-2-hydroxybenzamide (0.484 g, 2.00 mmol) in methylene chloride (35 mL) cooled to 0° C. was added 0.28 mL triethylamine (0.28 mL, 2.0 mmol), followed by the dropwise addition of a solution of 4-tert-butylbenzoyl chloride (0.393 mL, 2.00 mmol) in methylene chloride (15 mL). The reaction mixture was allowed to warm to room temperature over 16 h and washed with cold water. The organic layer was dried (magnesium sulfate), filtered, and concentrated in vacuo. Trituration with hexane provided 0.488 g (61%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313122B1
Source datasetuspto-grants-2001_11
ORD IDord-1d68e6b8ab8f45a9b1fa7d5183e1ca76
Source noteuspto-grants-2001_11