HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048853Generated: October 30, 2026
Benzylethanolamine → Ethyl (4-benzylmorpholin-2-yl)acetate
https://huagongshe.com/reaction/1048853
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylethanolamine | HCID 4348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl (E)-4-bromobut-2-enoate | HCID 5373944 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl (4-benzylmorpholin-2-yl)acetate | HCID 12582571 | 37.4% |
Reaction Steps
2-(Benzylamino)ethanol (19.05 ml, 132 mmol) and triethylamine (18.44 ml, 132 mmol) was added to water (150 ml) and the resulting mixture was heated to reflux temperature. (E)-Ethyl 4-bromobut-2-enoate (18.24 ml, 132 mmol) was added dropwise for 10 min The resulting mixture was further maintained at reflux temperature for 5 h. The reaction mixture was cooled to 25° C. and added NaOH (5.29 g, 132 mmol) after that the solvent was removed by distillation under reduced pressure to give orange oil. Ethyl acetate (150 mL) was added and the resulting solution was washed with water (2×50 mL). Ethyl acetate was distilled off under reduced pressure to give crude compound (15 g). This crude compound was purified by flash chromatography (Biotage) using eluent 20% ethyl acetate in hexane to yield 13 g of pure title compound as colorless viscous oil. m/z 264.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382216B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-a78af227dd354035adb7a0f759ac4a99 |
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| Source note | uspto-grants-2016_07 |
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