HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361865Generated: October 31, 2026
Triethylamine → N-(2,3-Epoxypropyl)-N-ethylaniline
https://huagongshe.com/reaction/2361865
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(N-ethylanilino)propane-1,2-diol | HCID 458693 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | N-(2,3-Epoxypropyl)-N-ethylaniline | HCID 89192 | 45% |
Reaction Steps
Methanesulfonyl chloride (2.5 mL, 1.5 eq.) was added to a solution 3-(ethyl-phenyl-amino)-propane-1,2-diol (4.22 g, 21.6 mmol) and triethylamine (9.03 mL, 3.0 eq.) in dichloromethane (20 mL) at −30 to −35° C. and the resulting mixture was stirred and warmed to 0° C. The reaction was quenched by sat. NaHCO3 (30 mL) and the separated aqueous phase was extracted with 2×20 mL CH2Cl2 and 20 mL EtOAc. The combined extracts were dried over Na2SO4, filtered and concentrated. The residue was dissolved in MeOH (30 mL) and treated with NaOMe (2.3 g, 2.0 eq.) at 65-70° C. for 3 h. After cooling to room temperature, the mixture was diluted with sat. NaHCO3 (50 mL) and extracted with 3×30 mL of EtOAc. The combined extracts were dried over Na2SO4, filtered and concentrated and the product was purified by chromatography (10% EtOAc/hexanes) to give ethyl-oxiranylmethyl-phenyl-amine (1.72 g, 45%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691814B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-d06f7c3d257840238353f3738c910c42 |
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| Source note | uspto-grants-2014_04 |
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