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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714177Generated: November 4, 2026

Acrylic Acid → HCID 20786195, compound

https://huagongshe.com/reaction/1714177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylic AcidHCID 6581—
Reactant4-MethylmorpholineHCID 7972—
ReactantIsobutyl chloroformateHCID 62365—
ReactantN-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
SolventDichloromethaneHCID 6344—
ProductHCID 20786195HCID 2078619534.3%

Reaction Steps

To a solution of acrylic acid (2.50 g, 34.7 mmol) in dichloromethane (80 mL) at 0 degrees Celcius was added N-methyl-morpholine (4.73 g, 46.8 mmol), followed by isobutyl chloroformate (6.37 g, 46.8 mmol). After 30 minutes, a solution of (2-amino-phenyl)-carbamic acid tertbutyl ester (5.80 g, 27.8 mmol) in dichloromethane (50 mL) was added dropwise to the refluxing reaction mixture over 30 min. After the reaction was completed (2 hours later), the reaction mixture was allowed to cool down to room temperature, poured into ice water, and extracted with dichloromethane (30 mL×3). The organic layer was washed with water, dilute sodium bicarbonate solution, 0.1M HCl, water, and brine in turn. The organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo. The crude solid was recrystallized from ethyl acetate/petroleum ether=1/4 (v/v) to obtain the desired product (2.5 g, 34%). MS: calc'd 263 (MH+), exp 263 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795315B2
Source datasetuspto-grants-2010_09
ORD IDord-2e4c7cedd3084aa9874bb4dce8cc04aa
Source noteuspto-grants-2010_09