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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407128Generated: October 27, 2026

Acryloyl chloride → Methyl 4-Acryloylamino-5-chloro-2-methoxybenzoate

https://huagongshe.com/reaction/407128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcryloyl chlorideHCID 13140—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 4-amino-5-chloro-2-methoxybenzoateHCID 700493—
SolventDichloromethaneHCID 6344—
ProductMethyl 4-Acryloylamino-5-chloro-2-methoxybenzoateHCID 2188061667%

Reaction Steps

To a 1-liter three-necked round-bottom flask equipped with overhead stirrer, temperature control and addition funnel was added methyl 4-amino-5-chloro-2-methoxybenzoate (44.2 g, 200 mmol), dichloromethane (500 mL) and diisopropylethylamine (104.5 mL, 600 mmol). The resulting mixture was stirred at room temperature until the ingredients dissolved and then the mixture was cooled to 0° C. Acryloyl chloride (16.25 mL, 200 mmol) was then added dropwise while maintaining the internal reaction mixture temperature below 10° C. The total time for addition was about 30 min. The reaction mixture was then slowly warmed from 0° C. to room temperature over a period of about 2 hours. Aqueous saturated sodium bicarbonate solution (200 mL) and dichloromethane (200 mL) were then added and this mixture was stirred for 15 min. and then the layers were separated. The dichloromethane layer was washed with 1 M hydrochloric acid (200 mL) and then concentrated under reduced pressure to about one-third its original volume resulting in a thick slurry. The slurry was filtered and the filter cake was washed with dichloromethane (100 mL) and dried to provide the title compound as an off-white solid (36 g, 67% yield, >98% purity by HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754223B2
Source datasetuspto-grants-2014_06
ORD IDord-89574fdd6e744409a0eaf5f0e5795212
Source noteuspto-grants-2014_06