HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254679Generated: October 25, 2026
Cyanamide → Ethyl 5-chloro-N-cyano-2-methoxybenzimidate
https://huagongshe.com/reaction/254679
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | Sodium Phosphate, Monobasic, Monohydrate | HCID 516949 | — |
| Reactant | Phosphoric acid, disodium salt, heptahydrate | HCID 6096963 | — |
| Reactant | Ethyl 5-chloro-2-methoxybenzimidate hydrochloride | HCID 66851771 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 5-chloro-N-cyano-2-methoxybenzimidate | HCID 86623446 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07875640B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-c99ce14ac92a491ca18385dac92c506d |
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| Source note | uspto-grants-2011_01 |
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