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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538820Generated: October 25, 2026

Cyanamide → Ethyl 5-chloro-N-cyano-2-methoxybenzimidate

https://huagongshe.com/reaction/538820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantSodium Phosphate, Monobasic, MonohydrateHCID 516949—
ReactantPhosphoric acid, disodium salt, heptahydrateHCID 6096963—
ReactantEthyl 5-chloro-2-methoxybenzimidate hydrochlorideHCID 66851771—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductEthyl 5-chloro-N-cyano-2-methoxybenzimidateHCID 8662344690%

Reaction Steps

A solution of ethyl 5-chloro-2-methoxybenzimidate (1.3 g, 6.2 mmol, obtained after aqueous bicarbonate wash of Example 93D) in acetonitrile (2 mL) was added to a solution of sodium phosphate monobasic monohydrate (3.4 g, 24.7 mmol), sodium phosphate dibasic heptahydrate (3.3 g, 12.4 mmol) and cyanamide (0.52 g, 12.4 mmol) in water (20 mL). The reaction mixture was stirred at room temperature for overnight and then extracted with CH2Cl2 (3×15 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated. The residue contained about 30% of starting material. The residue was reprocessed with half the amounts of the reagents to drive the reaction to completion and that yielded 1.32 g (90%) of the title compound. MS (ESI+) m/z 239 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865753B2
Source datasetuspto-grants-2014_10
ORD IDord-4184103ff16b4179bc5ddc0f13f68ec0
Source noteuspto-grants-2014_10