HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (2S)-3-(4-hydroxy-phenyl)-2-methoxypropionic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | (2S)-3-(4-hydroxyphenyl)-2-methoxypropanoic acid | HCID 11564639 | — |
| Product | (2S)-3-(4-hydroxy-phenyl)-2-methoxypropionic acid ethyl ester | HCID 11390460 | — |
Reaction Steps
A solution of (S)-3-(4-hydroxy-phenyl)-2-methoxy-propionic acid (20 g, 100 mmol) in 3 A ethanol (140 mL) was treated dropwise with concentrated sulfuric acid (5.7 mL)) and stirred at room temperature overnight. The solution was concentrated and is water (110 mL) was added. Sodium bicarbonate was added to bring the pH to 7–8. The mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were washed with 20% NaCl solution (50 ml), dried (MgSO4), filtered, and concentrated to a golden oil (18 g, 80%). 1H-NMR (CDCl3): 7.1(d, 2H); 6.7(d, 2H); 4.2(m, 2H); 3.9(m, 1H); 3.6(s, 3H); 2.95(m, 2H); 125(t, 3H). MS (ES): 223.2 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192982B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-936acab36d25451eaf54f1778e988164 |
| Source note | uspto-grants-2007_03 |