HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426868Generated: November 2, 2026
p-Toluenesulfonic acid → HCID 60135688, compound
https://huagongshe.com/reaction/1426868
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | 4-Amino-2,5-dimethylphenol | HCID 76544 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 60135688 | HCID 60135688 | 55% |
Reaction Steps
To a mixture of 10.0 g (73 mmol) of 4-amino-2,5-dimethylphenol and 73 ml (0.84 mol) of trimethoxymethane 0.73 g (4.2 mmol) of p-toluene sulfonic acid were added and the mixture was heated to reflux for 2 hours. Then the volatiles were removed in vacuo and the residue was dissolved in 73 ml of toluene and 12.9 g (217 mmol) N-methylethanamine were added. The reaction mixture was heated to 50° C. for 20 hrs and concentrated in vacuo. Column chromatographie (gradient: cyclohexane->ethyl acetate) yielded 9.17 g (44 mmol) 55% of N-ethyl-N′-(4-hydroxy-2,5-dimethylphenyl)-N-methylimidoformamide; log P (pH 2.3)=0.41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933107B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-75f6a5544d3b4f79997692e8cae5507c |
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| Source note | uspto-grants-2015_01 |
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