HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 2-(2,2-Dimethyl-1,3-dioxan-5-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Hydroxymethyl)butane-1,4-diol | HCID 11040684 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-(2,2-Dimethyl-1,3-dioxan-5-yl)ethanol | HCID 11816011 | 989.3% |
Reaction Steps
A solution of compound 31 (160 g, 1.30 mol) and 2,2′-dimethoxypropane (207 g, 1.90 mol) in dry acetone (800 mL) was added p-TsOH (92 g, 0.053 mol) under N2 and stirred at RT for 12 h. To this was added triethylamine drop-wise to neutral pH and then concentrated under vacuum below 35° C. The crude residue was purified by column chromatography over neutral alumina (12% ethyl acetate in pet ether) to give the title compound (84 g, 39%). TLC: Pet ether/EtOAc, 1:1, Rf=0.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795270B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-533e0bcfeaa64c9dbe0d0a6d7f5a7571 |
| Source note | uspto-grants-2010_09 |