HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020429Generated: November 1, 2026
O-Phenylenediamine → HCID 49805202, compound
https://huagongshe.com/reaction/1020429
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86663231 | HCID 86663231 | — |
| Reactant | HCID 178486080 | HCID 178486080 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 49805202 | HCID 49805202 | 52.2% |
Reaction Steps
Phenylenediamine (217 mg, 2.01 mmol), 1H-benzothiazol-1-yloxytris-(dimethylamino)phosphonium hexafluorophosphate (BOP; 667 mg, 1.51 mmol) and triethyl amine (203 mg, 2.01 mmol) were dissolved in 3 mL of DMF. 350 mg of the 4-((3-bromo-2-methylbenzamido)methyl)benzoate obtained in step 2 (1.01 mmol) was added thereto and stirred at room temperature overnight. The resulting mixture was subjected to thin layer chromatography to monitor the amount of 4-((3-bromo-2-methylbenzamido)methyl)benzoate consumed, and DMF was removed under a reduced pressure. 50 mL of saturated sodium bicarbonate was added to the resulting mixture, extracted with methylene chloride (3×75 mL) and the separated organic layer was dried over anhydrous magnesium sulfate. The residue was dissolved in methylene chloride and n-pentane was added thereto. The resulting solid thus obtained was filtered and washed with ethanol to obtain the title compound (231 mg, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716326B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-1ac68cab456b499fbfcfa0ce2efbf996 |
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| Source note | uspto-grants-2014_05 |
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