HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 5-(Chloromethyl)-1,2,3-trimethoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3,4,5-Trimethoxybenzyl alcohol | HCID 77449 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 5-(Chloromethyl)-1,2,3-trimethoxybenzene | HCID 77448 | — |
Reaction Steps
In 40 ml of benzene was dissolved 10 g of 3,4,5-trimethoxybenzyl alcohol. To the resulting solution was dropwise added under chilling with ice 10 mlof benzene solution containing 7.6 g of thionyl chloride. After the addition was complete, the mixture was stirred at room temperature for 15 min. The reaction solution was poured into a chilled aqueous potassium carbonate, and a separated benzene portion was collected. The benzene portion was washed with a saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and placed under reduced pressure to distill off the solvent. The desired compound was obtained as a yellow solid (yield: 11.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446146 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-abc788a9d2dc41f2844eee3125898d59 |
| Source note | uspto-grants-1995_08 |