HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481017Generated: October 30, 2026
Sodium Hydroxide → HCID 18765916, compound
https://huagongshe.com/reaction/481017
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18765895 | HCID 18765895 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 18765916 | HCID 18765916 | — |
Reaction Steps
The solution of ethyl 3-(2-{[2-(1-pyrrolidinyl)ethoxy]methyl}phenyl)propanoate (8.10 g, 26.5 mmol) in ethanol (40 ml) and 5N NaOH aq. solution (32.0 mmol, 6.4 ml) was stirred at room temperature for 15 h. The mixture was neutrallized with 1N HCl-ethanol (32 ml) at 0° C. The solvents were removed by simple distillation procedure at ˜1 atom (oil bath temperature; 105˜110° C.). The residue was then diluted with acetonitrile (50 ml) and then the solvents were removed by distillation (oil bath temperature; 105˜110° C.) for azeotropic removal of water and ethanol until inner temperature 79.5° C.˜80.5° C. The residue was then diluted with acetonitrile (60 ml) and dried over sodium sulfate. After filtration, the filtrate was evaporated in vacuo to afford the titled compound (quant.) as a dark yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653313B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-cb523ae6295f4999976efef26a98477f |
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| Source note | uspto-grants-2003_11 |
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