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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597482Generated: October 26, 2026

Pentachlorophenol → HCID 21445183, compound

https://huagongshe.com/reaction/597482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentachlorophenolHCID 992—
ReactantPotassium IodideHCID 4875—
ReactantOxetane, 3,3-bis(chloromethyl)-HCID 6550—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 21445183HCID 21445183—

Reaction Conditions

Temperature140 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014855
Source datasetuspto-grants-1977_03
ORD IDord-d838a6c2a1664f99aad229bea729c165
Source noteuspto-grants-1977_03