HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → [2-(Benzyloxy)-2-oxoethoxy]acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dioxane-2,6-dione | HCID 78232 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-(Benzyloxy)-2-oxoethoxy]acetic acid | HCID 15221624 | 100.2% |
Reaction Steps
Diglycolic anhydride (4.11 g, 31.9 mmol) was dissolved in methylene chloride and benzyl alcohol (3.3 g, 31.9 mmol) was added, followed by triethylamine (3.22 g, 31.9 mmol). The reaction mixture was stirred at room temperature for 4 hours. Toluene (20 mL) was added, volatiles were evaporated and the residue was dried on vacuum pump overnight to afford 7.17 g of the title compound as a colorless oil. 1H NMR (CDCl3, 300 MHz): δ4.17 (s, 2H), 4.26 (s, 2H), 5.18 (s, 2H), 7.21-7.42 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06469065B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-f6f35c36c17c4045a5181b8fce122529 |
| Source note | uspto-grants-2002_10 |