HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335002Generated: October 30, 2026
3,5-Dimethylaniline → HCID 24801206, compound
https://huagongshe.com/reaction/335002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Dimethylaniline | HCID 7949 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 24801206 | HCID 24801206 | 34.8% |
Reaction Steps
A mixture of 3,5-dimethyl-aniline (0.04 mol), 2-bromo-ethanol (0.033 mol) and K2CO3 (0.033 mol) in CH3CN (50 ml) was stirred at 80° C. for 12 hours. The reaction was cooled down to room temperature and the solvent was evaporated. The residue was taken up in CH2Cl2/CH3OH (95/5) and washed with a saturated solution of K2CO3 in water. The organic layer was separated, dried (over MgSO4), filtered and the solvent was evaporated until dryness. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 98/2/0.1; 20-45 μm). The pure fractions were collected and the solvent was evaporated, yielding 1.9 g of 2-(3,5-dimethyl-phenylamino)-ethanol (29%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883837B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3b21c6ed5deb4d38be41f6806e22c810 |
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| Source note | uspto-grants-2014_11 |
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