HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Acetoxy-(4-methoxy-phenyl)-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Methoxymandelic acid | HCID 112056 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetoxy-(4-methoxy-phenyl)-acetic acid | HCID 18456650 | 96.7% |
Reaction Steps
4-Methoxymandelic acid (5.00 g, 27.44 mmol) was dissolved in 100 mL of THF. To this solution was added acetic anhydride (2.85 mL, 30.18 mmol), followed by Et3N (10 mL). The resulting mixture was stirred at room temperature overnight, concentrated, re-suspended in water, and extracted with EtOAc. The combined organic phase was dried over Na2SO4, and concentrated to give 5.95 g yellow syrup as the intermediate 79a. 1H NMR (300 MHz, CDCl3) δ 7.38 (d, 2H, J=8.67 Hz), 6.90 (d, 2H, J=8.67 Hz), 5.87 (s, 1H), 3.80 (s, 3H), 2.16 (s, 3H). LCMS (ESI−) [M−H]/z Calc'd 223, found 223.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208500B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-c2e80a004ee54e5bbf0973a2c0752f42 |
| Source note | uspto-grants-2007_04 |