HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1535039Generated: October 26, 2026
Carbon Tetrachloride → 1,3,5-Trichloro-2-(2-chloroethoxy)benzene
https://huagongshe.com/reaction/1535039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-(2,4,6-Trichlorophenoxy)ethan-1-ol | HCID 96343 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3,5-Trichloro-2-(2-chloroethoxy)benzene | HCID 11276959 | 98% |
Reaction Steps
Into a three-necked, round-bottom flask fitted with a stirrer, thermometer, reflux condenser and dropping funnel was added 250 g of 96% 2-(2,4,6-trichlorophenoxy) ethanol, 250 ml carbon tetrachloride and 4 g of benzyl-trimethyl-ammonium chloride. The mixture was heated to 55° C. and 146 g thionyl chloride was added dropwise over 1.5 hours. After the addition of the thionyl chloride the temperature of the reaction was slowly raised to 80° C. for a total reaction tme of 2.5 to 3 hours. The end of the reaction was determined by GLC. The mixture was cooled to 60° C. and water slowly added to decompose the excess thionyl chloride. The phases were separated and the organic phase was washed with a 10% sodium hydroxide solution until it reached a pH of 7. After an additional separation of the phases the organic phase was washed again with water. After a further separation of phases, the carbon tetrachloride was distilled off to yield an oil which slowly crystallized to form 257 g of 2-(2,4,6-trichlorophenoxy)-ethyl chloride in a purity of 96%-98% and yield of 98%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05091578 |
|---|
| Source dataset | uspto-grants-1992_02 |
|---|
| ORD ID | ord-83e99dc639134bbfa83ebdc2cc54716a |
|---|
| Source note | uspto-grants-1992_02 |
|---|