HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanediol → 2-Chloromethyl-2-(2,5-dimethylphenyl)-[1,3]dioxane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Reactant | 2-Chloro-1-(2,5-dimethylphenyl)ethan-1-one | HCID 2363693 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-Chloromethyl-2-(2,5-dimethylphenyl)-[1,3]dioxane | HCID 16050137 | — |
Reaction Steps
A mixture of 18.3 g [0.1 mol] of 2-chloro-1-(2,5-dimethylphenyl)ethanone, 15.2 g [0.2 mol] of trimethylene glycol, 1.9 g [0.01 mol] of p-TsOH hydrate and 150 ml of xylene is heated to boiling with a water trap for about 5 hours. Part of the xylene is then distilled off, and the reaction mixture is extracted at room temperature with 30 ml of saturated aqueous NaCl solution and twice with 100 ml of water each time. The organic phase is dried over sodium sulfate and concentrated in vacuo, and all volatiles are distilled off up to about 87° C. under 0.25 mbar. 22.9 g of residue remain with, according to GC, 83.9% product (79.8% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579500B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-0b80a20ace484d69aa2ab34a6a9d32e7 |
| Source note | uspto-grants-2009_08 |