HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(Chloromethyl)-2,3-bis{[2-(methyloxy)ethyl]oxy}benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2,3-Bis{[2-(methyloxy)ethyl]oxy}phenyl)methanol | HCID 66889790 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Chloromethyl)-2,3-bis{[2-(methyloxy)ethyl]oxy}benzene | HCID 66891310 | 96% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a solution of (2,3-bis{[2-(methyloxy)ethyl]oxy}phenyl)methanol (1.12 g, 4.37 mmol) and triethylamine (0.49 g, 4.84 mmol) in dichloromethane (20 mL) was slowly added thionyl chloride (0.78 g, 6.58 mmol) at 0° C. The solution was stirred at 0° C. for 15 min, and then at rt for 3 h. Dichloromethane (80 mL) was added, the solution was washed with water (50 mL), sat. sodium bicarbonate (50 mL), and brine (50 mL), dried with sodium sulfate, and concentrated to give crude 1-(chloromethyl)-2,3-bis{[2-(methyloxy)-ethyl]oxy}benzene (1.15 g, 96% yield) as a yellow oil. 1H NMR (400 MHz, CDCl3) δ7.02 (m, 2H), 6.90 (dd, 1H), 4.72 (s, 2H), 4.27 (m, 2H), 4.14 (m, 2H), 3.77 (m, 2H), 3.73 (m, 2H), 3.46 (s, 3H), 3.44 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07872014B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-cc1deea9b25949c18538cc00c06bfae1 |
| Source note | uspto-grants-2011_01 |