HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (R)-Methyl 2-(3-chlorophenyl)-2-hydroxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | (R)-2-(3-Chlorophenyl)-2-hydroxyacetic acid | HCID 2733127 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | (R)-Methyl 2-(3-chlorophenyl)-2-hydroxyacetate | HCID 15606324 | 93% |
Reaction Steps
A solution of (R)-2-(3-chlorophenyl)-2-hydroxyacetic acid (25 g, 133.69 mmol, 1.00 equiv.) in methanol (300 mL) and sulfuric acid (3 mL) was heated at reflux for about 16 hours, and then concentrated in vacuo. After the solution was poured into a water/ice mixture (200 mL), the pH value of the solution was adjusted to 9 with sodium carbonate. Standard extractive workup with ethyl acetate (2×100 mL), gave the title product as an off-white solid (24.8 g; yield=93%). 1H NMR (300 MHz, CDCl3) δ: 7.45 (s, 1H), 7.32 (m, 3H), 5.17 (d, J=4.5 Hz, 1H), 3.80 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778998B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-ef44bfaea98149bca2875ee49b8b94a5 |
| Source note | uspto-grants-2014_07 |