HuagongsheHuagongshe Chemistry Print Report · For research reference only
m-Chloroperbenzoic acid → Ethyl 2-(4-acetoxy-2-methylphenoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Ethyl 2-(4-acetyl-2-methylphenoxy)acetate | HCID 21986544 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-(4-acetoxy-2-methylphenoxy)acetate | HCID 21986316 | 72% |
Reaction Steps
A solution of ethyl 2-(4-acetyl-2-methylphenoxy)acetate (683) (8.78 g, 37 mmol), mCPBA (2.eq.), and p-TsOH monohydrate (0.15 eq.) in dichloromethane (160 mL) was heated at 40° C. overnight. The reaction was cooled to room temperature and washed with 1M KI (2×200 mL), 5% NaHSO3 (2×150 mL), and water (200 mL). The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by silica gel chromatography (0-100% EtOAc in hexanes) to provide ethyl 2-(4-acetoxy-2-methylphenoxy)acetate (684) (72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08309600B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-dd2385d01ee04876967d0fff27a927b8 |
| Source note | uspto-grants-2012_11 |