HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 57429413, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Florhydral | HCID 86209 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 57429413 | HCID 57429413 | 97% |
Reaction Steps
Ethylene glycol (18 mL, 0.32 mol, 1.2 eq), paratoluene sulfonic acid (400 mg, 1% w/w) and cyclohexane (50 mL) were charged into a 1 L three-necked round-bottom flask, equipped with a dean and stark, a reflux condenser and a mechanical stirrer. Florhydral™ 3-(3-isopropylphenyl)butanal, 49.3 g, 0.26 mol) was added dropwise at ambient temperature. The stirred mixture was then heated for 3 h at reflux. The reaction mixture was cooled at ambient temperature and washed water (2×100 mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled with a Vigreux column (7.2 mBar, 146° C.), to give 2-[2-(3-isopropylphenyl)propyl]-1,3-dioxolane (239 g, gc purity>98%; yield 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08709994B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-a9ecb8ca7cb04a21ac02f1495d955dd6 |
| Source note | uspto-grants-2014_04 |