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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096036Generated: November 1, 2026

Benzoyl chloride → HCID 23093472, compound

https://huagongshe.com/reaction/2096036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant2-(Methylamino)ethanolHCID 8016—
ReactantEthyl AcetateHCID 8857—
ReactantDi-tert-butyl dicarbonateHCID 90495—
SolventPyridineHCID 1049—
ProductHCID 23093472HCID 2309347266.5%

Reaction Steps

To a mixture of 2-(methylamino)ethanol (30.04 g) and ethyl acetate (90 mL) was added a mixture of di-tert-butyl dicarbonate (87.30 g) and ethyl acetate (10 mL) under ice-cooling. The reaction solution was stirred at room temperature for 1 hr, and benzoyl chloride (61.8 g) and pyridine (38.8 mL) were added thereeto under ice-cooling. The reaction solution was stirred at room temperature for 1 hr, and solid was filtered off. The solid was washed with ethyl acetate (100 mL), and the filtrate and washings were combined and washed with water (100 mL), then saturated saline (100 mL). The solution was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (100 mL), and added 4N hydrogen chloride-ethyl acetate solution (200 mL), followed by stirring at room temperature for 30 minutes. Diethyl ether (100 mL) was added thereto, and solid was collected by filtration. After washing two times with ethyl acetate (100 mL), the solid was dried at 60° C. under reduced pressure to give title compound as white solid (57.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449911B2
Source datasetuspto-grants-2013_05
ORD IDord-ee0f9e4719044a7a8b741cc8912468a6
Source noteuspto-grants-2013_05