HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Ethyl 3-(2-benzyloxy-ethoxy)-propionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Benzyloxyethanol | HCID 19595026 | — |
| Product | Ethyl 3-(2-benzyloxy-ethoxy)-propionate | HCID 66731906 | — |
Reaction Steps
8.53 ml (60.0 mmol) benzyloxy-ethanol are combined with 13 mg (0.57 mmol) sodium in 40 ml THF, then when it has dissolved 5.95 ml (54.7 mmol) ethyl acrylate are added under an argon atmosphere and stirred for 20 hours at ambient temperature. After neutralising with 0.6 ml 1-molar hydrochloric acid the reaction mixture is evaporated down i. vac., the residue is taken up in sat. sodium chloride solution and extracted with ethyl acetate. The combined organic phases are washed with sat. sodium chloride solution, dried over sodium sulphate and evaporated down i. vac. The residue is purified by chromatography on silica gel (eluant: petroleum ether/ethyl acetate=4:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07947700B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-198e62097ab64a0dac63cffb0a7eab82 |
| Source note | uspto-grants-2011_05 |