HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1,3-Diphenoxypropan-2-yl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Diphenoxy-2-propanol | HCID 12140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Diphenoxypropan-2-yl acetate | HCID 243013 | 45.3% |
Reaction Steps
9.6 g (39.3 mmol) of 2-hydroxy-1,3-diphenoxypropane are dissolved in 80 ml of tetrahydrofurane (THF) and cooled by an ice bath. To the solution are added dropwise 6.8 g (86.4 mmol) of acetyl chloride and 6.0 g (59.0 mmol) of triethylamine successively. The reaction mixture is stirred at room temperature overnight, poured into 50 ml of water, and extracted with ethyl acetate. The organic phase is washed with water and brine, dried over MgSO4, and concentrated. The residue is purified by flash chromatography on silica gel with ethyl acetate and hexane (1:9) as eluent, yielding 5.1 g of 2-acetyloxy-1,3-diphenoxypropane as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244544B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-732f28fd76fc4044b6c61066b793fed1 |
| Source note | uspto-grants-2007_07 |