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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593758Generated: November 3, 2026

Cyanoacetic acid → 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide

https://huagongshe.com/reaction/1593758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantDiisopropylcarbodiimideHCID 12734—
Reactant2,4-Dichloro-5-methoxyanilineHCID 1476636—
SolventTetrahydrofuranHCID 8028—
Product2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamideHCID 1609917888%

Reaction Conditions

Temperature15 °C

Reaction Steps

2,4-Dichloro-5-methoxyaniline (5.00 g, 26 mmol) and cyanoacetic acid (2.28 g, 26.8 mmol) were mixed in 50 mL of tetrahydrofuran until a solution formed. This solution was heated to reflux and 1,3-diisopropylcarbodiimide (4.2 mL, 26.8 mmol) was added dropwise. After 30 minutes the mixture was cooled to ˜15° C. in an ice-bath. The solid was collected by filtration and washed with tetrahydrofuran. The filtrate was slowly poured into water and stirred for 30 minutes. The white solid was collected by filtration, washed with water, and was then dissolved in 500 mL of ethyl acetate. The solution was dried over sodium sulfate and concentrated in vacuo to give 5.9 g (88%) of 2-cyano-N-(2,4-dichloro-5-methoxyphenyl)acetamide as a white solid, mp 180-181° C.; 1H NMR (400 MHz, DMSO-d6) δ 3.84 (s, 3H), 4.02 (s, 2H), 7.58 (s, 1 H), 7.66 (s, 1 H), 10.00 (s, 1 H); MS (ES) m/z257.0, 259.0 (M−H)−

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297795B2
Source datasetuspto-grants-2007_11
ORD IDord-b024c98b5b13422cb82bee4b7cd19512
Source noteuspto-grants-2007_11