HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597482Generated: October 26, 2026
Pentachlorophenol → HCID 21445183, compound
https://huagongshe.com/reaction/597482
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentachlorophenol | HCID 992 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Oxetane, 3,3-bis(chloromethyl)- | HCID 6550 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21445183 | HCID 21445183 | — |
Reaction Steps
This reaction was carried out similarly to that described in Example 1. Pentachlorophenol (469 g., 1.86 moles), potassium carbonate (262 g., 1.9 moles), potassium iodide (4 g.) and 1.5 liters of dimethyl formamide were charged to a 3 liter reaction flask. The mixture was stirred and heated in a nitrogen atmosphere. When the temperature reached 95° C., 140 g. (0.9 moles) of 3,3-bischloromethyl oxetane was added. The reaction mixture was slowly heated to about 140° C. and held 3 hours. After cooling to 63° C., 700 ml. of water was added to the mixture. After standing overnight, the reaction mixture was filtered. The recovered crystalline 3,3-bis[pentachlorophenoxymethyl]oxetane was washed on the funnel with six portions of water, three portions of ethanol and three portions of 2-butanone. The yield of oven-dried, cream-colored crystals was 480 g. (87%). The compound melted at 229°-230° C. If desired, this compound can be recrystallized from dioxane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04014855 |
|---|
| Source dataset | uspto-grants-1977_03 |
|---|
| ORD ID | ord-d838a6c2a1664f99aad229bea729c165 |
|---|
| Source note | uspto-grants-1977_03 |
|---|